Friday, September 30, 2016

Xanax XR


See also: Generic Xanax


Xanax XR is a brand name of alprazolam, approved by the FDA in the following formulation(s):


XANAX XR (alprazolam - tablet, extended release; oral)



  • Manufacturer: PHARMACIA AND UPJOHN

    Approval date: January 17, 2003

    Strength(s): 0.5MG [AB], 1MG [AB], 2MG [AB], 3MG [RLD][AB]

Has a generic version of Xanax XR been approved?


Yes. The following products are equivalent to Xanax XR:


alprazolam tablet, extended release; oral



  • Manufacturer: ACTAVIS ELIZABETH

    Approval date: February 13, 2007

    Strength(s): 0.5MG [AB], 1MG [AB], 2MG [AB], 3MG [AB]


  • Manufacturer: AMNEAL PHARMS NY

    Approval date: May 30, 2008

    Strength(s): 0.5MG [AB], 1MG [AB], 2MG [AB], 3MG [AB]


  • Manufacturer: ANCHEN PHARMS

    Approval date: September 29, 2011

    Strength(s): 0.5MG [AB], 1MG [AB], 2MG [AB], 3MG [AB]


  • Manufacturer: APOTEX INC

    Approval date: November 12, 2008

    Strength(s): 0.5MG [AB], 2MG [AB], 3MG [AB]


  • Manufacturer: AUROBINDO PHARMA USA

    Approval date: June 7, 2011

    Strength(s): 0.5MG [AB], 1MG [AB], 2MG [AB], 3MG [AB]


  • Manufacturer: BARR

    Approval date: July 31, 2006

    Strength(s): 0.5MG [AB], 1MG [AB], 2MG [AB], 3MG [AB]


  • Manufacturer: COREPHARMA

    Approval date: January 31, 2007

    Strength(s): 0.5MG [AB], 1MG [AB], 2MG [AB], 3MG [AB]


  • Manufacturer: IMPAX LABS

    Approval date: May 24, 2007

    Strength(s): 0.5MG [AB], 1MG [AB], 2MG [AB], 3MG [AB]


  • Manufacturer: MYLAN

    Approval date: January 26, 2006

    Strength(s): 0.5MG [AB], 1MG [AB], 2MG [AB], 3MG [AB]


  • Manufacturer: SANDOZ

    Approval date: June 30, 2006

    Strength(s): 0.5MG [AB], 1MG [AB], 2MG [AB], 3MG [AB]


  • Manufacturer: TEVA PHARMS

    Approval date: February 28, 2007

    Strength(s): 0.5MG [AB], 1MG [AB], 2MG [AB], 3MG [AB]


  • Manufacturer: VINTAGE

    Approval date: October 15, 2007

    Strength(s): 0.5MG [AB], 1MG [AB], 2MG [AB], 3MG [AB]


  • Manufacturer: WATSON LABS FLORIDA

    Approval date: May 13, 2010

    Strength(s): 0.5MG [AB], 1MG [AB], 2MG [AB], 3MG [AB]


  • Manufacturer: ZYDUS PHARMS USA INC

    Approval date: October 17, 2008

    Strength(s): 0.5MG [AB], 1MG [AB], 2MG [AB], 3MG [AB]

Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Xanax XR. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents

There are no current U.S. patents associated with Xanax XR.

See also...

  • Xanax XR Consumer Information (Drugs.com)
  • Xanax XR Extended-Release Tablets Consumer Information (Wolters Kluwer)
  • Xanax XR Consumer Information (Cerner Multum)
  • Xanax XR Advanced Consumer Information (Micromedex)
  • Alprazolam Consumer Information (Drugs.com)
  • Alprazolam Consumer Information (Wolters Kluwer)
  • Alprazolam Extended-Release Tablets Consumer Information (Wolters Kluwer)
  • Alprazolam Orally Disintegrating Tablets Consumer Information (Wolters Kluwer)
  • Alprazolam Solution Consumer Information (Wolters Kluwer)
  • Alprazolam Consumer Information (Cerner Multum)
  • Alti-Alprazolam Advanced Consumer Information (Micromedex)
  • Gabazolamine-0.5 Advanced Consumer Information (Micromedex)
  • Alprazolam Advanced Consumer Information (Micromedex)
  • Alprazolam AHFS DI Monographs (ASHP)

Janumet


Janumet is a brand name of metformin/sitagliptin, approved by the FDA in the following formulation(s):


JANUMET (metformin hydrochloride; sitagliptin phosphate - tablet; oral)



  • Manufacturer: MERCK

    Approval date: March 30, 2007

    Strength(s): 1GM;EQ 50MG BASE [RLD], 500MG;EQ 50MG BASE

Has a generic version of Janumet been approved?


No. There is currently no therapeutically equivalent version of Janumet available.


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Janumet. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents


Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.




  • Use of dipeptidyl peptidase IV effectors for lowering the blood glucose level in mammals
    Patent 6,303,661
    Issued: October 16, 2001
    Inventor(s): Demuth; Hans-Ulrich & Rosche; Fred & Schmidt; Joem & Pauly; Robert P. & McIntosh; Christopher H. S. & Pederson; Ray A.
    Assignee(s): Probiodrug
    Novel therapeutic regimens are provided which comprise the administration of therapeutically effective amounts of an inhibitor to dipeptidyl peptidase (DP-IV) or enzymes of similar activity whereby their ability to degrade the incretins, GLP-1 and GIP, is reduced. As a result hyperglycemia, such as that accompanying food intake may be reduced due to improved insulin release. A preferred therapeutic regimen amongst a number of routes of administration and inhibitors that may be used comprises the oral administration of isoleucyl thiazolidine.
    Patent expiration dates:

    • April 24, 2017
      ✓ 
      Patent use: METHOD OF TREATING TYPE 2 DIABETES MELLITUS BY ADMINISTERING A DIPEPTIDYL PEPTIDASE-IV INHIBITOR




  • Beta-amino heterocyclic dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes
    Patent 6,699,871
    Issued: March 2, 2004
    Inventor(s): Scott D.; Edmondson & Michael H.; Fisher & Dooseop; Kim & Malcolm; Maccoss & Emma R.; Parmee & Ann E.; Weber & Jinyou; Xu
    Assignee(s): Merck & Co., Inc.
    The present invention is directed to compounds which are inhibitors of the dipeptidyl peptidase-IV enzyme (“DP-IV inhibitors”) and which are useful in the treatment or prevention of diseases in which the dipeptidyl peptidase-IV enzyme is involved, such as diabetes and particularly type 2 diabetes. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which the dipeptidyl peptidase-IV enzyme is involved.
    Patent expiration dates:

    • July 26, 2022
      ✓ 
      Patent use: METHOD OF TREATING TYPE 2 DIABETES MELLITUS BY ADMINISTERING A DIPEPTIDYL PEPTIDASE-IV INHIBITOR
      ✓ 
      Drug substance
      ✓ 
      Drug product




  • Method of regulating glucose metabolism, and reagents related thereto
    Patent 6,890,898
    Issued: May 10, 2005
    Inventor(s): Bachovchin; William W. & Plaut; Andrew G. & Drucker; Daniel
    Assignee(s): Trustees of Tufts College
    1149336 Ontario Inc.
    New England Medical Center Hospitals, Inc.
    The present invention provides methods and compositions for modification and regulation of glucose and lipid metabolism, generally to reduce insulin resistance, hyperglycemia, hyperinsulinemia, obesity, hyperlipidemia, hyperlipoprotein-emia (such as chylomicrons, VLDL and LDL), and to regulate body fat and more generally lipid stores, and, more generally, for the improvement of metabolism disorders, especially those associated with diabetes, obesity and/or atherosclerosis.
    Patent expiration dates:

    • February 2, 2019
      ✓ 
      Patent use: METHOD OF TREATING TYPE 2 DIABETES MELLITUS BY ADMINISTERING A DIPEPTIDYL PEPTIDASE-IV INHIBITOR IN COMBINATION WITH METFORMIN


    • February 2, 2019
      ✓ 
      Patent use: METHOD OF TREATING TYPE 2 DIABETES MELLITUS BY ADMINISTERING A DIPEPTIDYL PEPTIDASE-4 INHIBITOR IN COMBINATION WITH METFORMIN AND A PPAR-GAMMA AGONIST


    • February 2, 2019
      ✓ 
      Patent use: METHOD OF TREATING TYPE 2 DIABETES MELLITUS BY ADMINISTERING A DIPEPTIDYL PEPTIDASE-4 INHIBITOR IN COMBINATION WITH INSULIN




  • Method of regulating glucose metabolism, and reagents related thereto
    Patent 7,078,381
    Issued: July 18, 2006
    Inventor(s): Bachovchin; William W. & Plaut; Andrew G. & Drucker; Daniel
    Assignee(s): Trustees of Tufts College
    The present invention provides methods and compositions for modifying glucose metabolism and treating Type II diabetes in an animal, along with modifying metabolism of a peptide hormone in an animal. Compositions disclosed herein comprise one or more peptides and/or peptide analogs which include a functional group that reacts with an active site residue of a protease.
    Patent expiration dates:

    • February 2, 2019
      ✓ 
      Patent use: METHOD OF TREATING TYPE 2 DIABETES MELLITUS BY ADMINISTERING A DIPEPTIDYL PEPTIDASE-IV INHIBITOR IN COMBINATION WITH METFORMIN


    • February 2, 2019
      ✓ 
      Patent use: METHOD OF TREATING TYPE 2 DIABETES MELLITUS BY ADMINISTERING A DIPEPTIDYL PEPTIDASE-4 INHIBITOR IN COMBINATION WITH INSULIN


    • February 2, 2019
      ✓ 
      Patent use: METHOD OF TREATING TYPE 2 DIABETES MELLITUS BY ADMINISTERING A DIPEPTIDYL PEPTIDASE-4 INHIBITOR IN COMBINATION WITH METFORMIN AND A PPAR-GAMMA AGONIST




  • Beta-amino tetrahydroimidazo (1, 2-a) pyrazines and tetrahydrotrioazolo (4, 3-a) pyrazines as dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes
    Patent 7,125,873
    Issued: October 24, 2006
    Inventor(s): Edmondson; Scott D & Fisher; Michael H. & Kim; Dooseop & Maccoss; Malcolm & Parmee; Emma R. & Weber; Ann E & Xu; Jinyou
    Assignee(s): Merck & Co., Inc.
    The present invention is directed to compounds which are inhibitors of the dipeptidyl peptidase-IV enzyme (“DP-IV inhibitors”) and which are useful in the treatment or prevention of diseases in which the dipeptidyl peptidase-IV enzyme is involved, such as diabetes and particularly type 2 diabetes. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which the dipeptidyl peptidase-IV enzyme is involved.
    Patent expiration dates:

    • July 26, 2022
      ✓ 
      Patent use: METHOD OF TREATING TYPE 2 DIABETES MELLITUS BY ADMINISTERING A DIPEPTIDYL PEPTIDASE-IV INHIBITOR IN COMBINATION WITH METFORMIN
      ✓ 
      Drug product


    • July 26, 2022
      ✓ 
      Patent use: METHOD OF TREATING TYPE 2 DIABETES MELLITUS BY ADMINISTERING A DIPEPTIDYL PEPTIDASE-4 INHIBITOR IN COMBINATION WITH METFORMIN AND A PPAR-GAMMA AGONIST
      ✓ 
      Drug product


    • July 26, 2022
      ✓ 
      Patent use: METHOD OF TREATING TYPE 2 DIABETES MELLITUS BY ADMINISTERING A DIPEPTIDYL PEPTIDASE-4 INHIBITOR IN COMBINATION WITH INSULIN
      ✓ 
      Drug product




  • Phosphoric acid salt of a dipeptidyl peptidase-IV inhibitor
    Patent 7,326,708
    Issued: February 5, 2008
    Inventor(s): Cypes; Stephen Howard & Chen; Alex Minhua & Ferlita; Russell R. & Hansen; Karl & Lee; Ivan & Vydra; Vicky K. & Wenslow, Jr.; Robert M.
    Assignee(s): Merck & Co., Inc.
    The dihydrogenphosphate salt of 4-oxo-4-[3-(trifluoromethyl)-5,6-dihydro [1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl]-1-(2,4,5-trifluorophenyl)butan-2-amine is a potent inhibitor of dipeptidyl peptidase-IV and is useful for the prevention and/or treatment of non-insulin dependent diabetes mellitus, also referred to as type 2 diabetes. The invention also relates to a crystalline monohydrate of the dihydrogenphosphate salt as well as a process for its preparation, pharmaceutical compositions containing this novel form and methods of use for the treatment of diabetes, obesity, and high blood pressure.
    Patent expiration dates:

    • April 11, 2026
      ✓ 
      Patent use: METHOD OF TREATING TYPE 2 DIABETES MELLITUS BY ADMINISTERING A DIPEPTIDYL PEPTIDASE-IV INHIBITOR
      ✓ 
      Drug substance
      ✓ 
      Drug product



Related Exclusivities

Exclusivity is exclusive marketing rights granted by the FDA upon approval of a drug and can run concurrently with a patent or not. Exclusivity is a statutory provision and is granted to an NDA applicant if statutory requirements are met.

  • Exclusivity expiration dates:
    • October 12, 2010 - DESCRIPTION OF RESULTS OF STUDY OF INITIAL THERAPY IN COMBINATION WITH METFORMIN WHEN DIET AND EXERCISE DO NOT PROVIDE GLYCEMIC CONTROL

    • October 12, 2010 - RESULTS OF STUDY OF COMBINATION THERAPY AND NON-INFERIORITY STUDY

    • October 16, 2011 - NEW CHEMICAL ENTITY

See also...

  • Janumet Consumer Information (Drugs.com)
  • Janumet Consumer Information (Wolters Kluwer)
  • Janumet Consumer Information (Cerner Multum)
  • Janumet Advanced Consumer Information (Micromedex)
  • Sitagliptin/Metformin Consumer Information (Wolters Kluwer)
  • Metformin and sitagliptin Consumer Information (Cerner Multum)
  • Metformin and sitagliptin Advanced Consumer Information (Micromedex)
  • Sitagliptin and metformin Advanced Consumer Information (Micromedex)

Nordette-28


Nordette-28 is a brand name of ethinyl estradiol/levonorgestrel, approved by the FDA in the following formulation(s):


NORDETTE-28 (ethinyl estradiol; levonorgestrel - tablet; oral-28)



  • Manufacturer: DURAMED

    Approval date: July 21, 1982

    Strength(s): 0.03MG;0.15MG [RLD][AB]

Has a generic version of Nordette-28 been approved?


Yes. The following products are equivalent to Nordette-28:


ALTAVERA (ethinyl estradiol; levonorgestrel tablet; oral-28)



  • Manufacturer: SANDOZ

    Approval date: August 3, 2010

    Strength(s): 0.03MG;0.15MG [AB]

LEVORA 0.15/30-28 (ethinyl estradiol; levonorgestrel tablet; oral-28)



  • Manufacturer: WATSON LABS

    Approval date: December 13, 1993

    Strength(s): 0.03MG;0.15MG [AB]

PORTIA-28 (ethinyl estradiol; levonorgestrel tablet; oral-28)



  • Manufacturer: BARR

    Approval date: May 23, 2002

    Strength(s): 0.03MG;0.15MG [AB]

Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Nordette-28. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents

There are no current U.S. patents associated with Nordette-28.

See also...

  • Levonorgestrel/Ethinyl Estradiol Consumer Information (Wolters Kluwer)
  • Ethinyl estradiol and levonorgestrel Consumer Information (Cerner Multum)
  • Ethinyl estradiol and levonorgestrel extended-cycle Consumer Information (Cerner Multum)

Propecia


Propecia is a brand name of finasteride, approved by the FDA in the following formulation(s):


PROPECIA (finasteride - tablet; oral)



  • Manufacturer: MERCK

    Approval date: December 19, 1997

    Strength(s): 1MG [RLD][AB]

Has a generic version of Propecia been approved?


A generic version of Propecia has been approved by the FDA. However, this does not mean that the product will necessarily be commercially available - possibly because of drug patents and/or drug exclusivity. The following products are equivalent to Propecia and have been approved by the FDA:


finasteride tablet; oral



  • Manufacturer: DR REDDYS LABS INC

    Approval date: July 28, 2006

    Strength(s): 1MG [AB]

Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Propecia. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents


Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.




  • Method of treating androgenic alopecia with 5-.alpha. reductase inhibitors
    Patent 5,547,957
    Issued: August 20, 1996
    Inventor(s): Gormley; Glenn J. & Kaufman; Keith D. & Stoner; Elizabeth & Waldstreicher; Joanne
    Assignee(s): Merck & Co., Inc.
    The instant invention involves a method of treating and/or reversing androgenic alopecia and promoting hair growth, and methods of treating acne vulgaris, seborrhea, and female hirsutism, by administering to a patient in need of such treatment a 5.alpha.-reductase 2 inhibitor, such as finasteride, in a dosage amount under 5 mgs/day.
    Patent expiration dates:

    • October 15, 2013
      ✓ 
      Patent use: TREATING MALE PATTERN BALDNESS WITH 0.05 TO 3.0MG/DAY




  • Methods of treating androgenic alopecia with finasteride [17.beta.-N-mono-substituted-carbamoyl-4-aza-5-.alpha.-androst-1-en-ones]
    Patent 5,571,817
    Issued: November 5, 1996
    Inventor(s): Rasmusson; Gary H. & Reynolds; Glenn F.
    Assignee(s): Merck & Co., Inc.
    17.beta.-N-monosubstituted-carbamoyl-4-5.alpha.-androst-1-en-3-ones of the formula ##STR1## wherein R.sup.1 is selected from hydrogen, methyl and ethyl and R.sup.2 is a branched chain alkyl of from 3-12 carbons, and R', R", R'" are hydrogen or methyl are active as testosterone 5.alpha.-reductase inhibitors and thus are useful topically for treatment of androgenic alopecia.
    Patent expiration dates:

    • November 5, 2013
      ✓ 
      Patent use: TREATMENT OF ANDROGENIC ALOPECIA BY ORAL ADMINISTRATION DRUG SUBSTANCE




  • Finasteride processes
    Patent 5,886,184
    Issued: March 23, 1999
    Inventor(s): Dolling; Ulf H. & McCauley; James A. & Varsolona; Richard J.
    Assignee(s): Merck & Co., Inc.
    Disclosed is a new process for producing finasteride which involves reacting the magnesium halide salt of 17.beta.-carboalkoxy-4-aza-5.alpha.-androst-1-en-3-one with t-butylamino magnesium halide, present in at least a 2:1 molar ratio to the ester, formed from t-butyl amine and an aliphatic/aryl magnesium halide at ambient temperature in an inert organic solvent under an inert atmosphere followed by heating and recovering the product finasteride. Also disclosed are two polymorphic crystalline Forms I and II of finasteride, and methods of their production.
    Patent expiration dates:

    • November 19, 2012



See also...

  • Propecia Consumer Information (Drugs.com)
  • Propecia Consumer Information (Wolters Kluwer)
  • Propecia Consumer Information (Cerner Multum)
  • Propecia Advanced Consumer Information (Micromedex)
  • Finasteride Consumer Information (Wolters Kluwer)
  • Finasteride Consumer Information (Cerner Multum)
  • Finasteride Advanced Consumer Information (Micromedex)
  • Finasteride AHFS DI Monographs (ASHP)

Beta-Val


Beta-Val is a brand name of betamethasone topical, approved by the FDA in the following formulation(s):


BETA-VAL (betamethasone valerate - cream; topical)



  • Manufacturer: TEVA

    Approval date: March 24, 1983

    Strength(s): EQ 0.1% BASE [AB]

Has a generic version of Beta-Val been approved?


Yes. The following products are equivalent to Beta-Val:


DERMABET (betamethasone valerate cream; topical)



  • Manufacturer: TARO

    Approval date: January 6, 1988

    Strength(s): EQ 0.1% BASE [AB]

VALNAC (betamethasone valerate cream; topical)



  • Manufacturer: ACTAVIS MID ATLANTIC

    Approval date: October 10, 1984

    Strength(s): EQ 0.1% BASE [AB]

Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Beta-Val. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents

There are no current U.S. patents associated with Beta-Val.

See also...

  • Beta-Val Cream Consumer Information (Wolters Kluwer)
  • Beta-Val Lotion Consumer Information (Wolters Kluwer)
  • Beta-Val Consumer Information (Cerner Multum)
  • Beta-Val Advanced Consumer Information (Micromedex)
  • Betamethasone Dipropionate (Augmented) Cream Consumer Information (Wolters Kluwer)
  • Betamethasone Dipropionate (Augmented) Lotion Consumer Information (Wolters Kluwer)
  • Betamethasone Dipropionate Cream Consumer Information (Wolters Kluwer)
  • Betamethasone Dipropionate Gel Consumer Information (Wolters Kluwer)
  • Betamethasone Dipropionate Lotion Consumer Information (Wolters Kluwer)
  • Betamethasone Valerate Cream Consumer Information (Wolters Kluwer)
  • Betamethasone Valerate Foam Consumer Information (Wolters Kluwer)
  • Betamethasone Valerate Lotion Consumer Information (Wolters Kluwer)
  • Betamethasone topical Consumer Information (Cerner Multum)
  • Celestoderm-V Advanced Consumer Information (Micromedex)
  • Celestoderm-V/2 Advanced Consumer Information (Micromedex)
  • Dovobet Advanced Consumer Information (Micromedex)
  • Ectosone Mild-Lotion Advanced Consumer Information (Micromedex)
  • Ectosone Regular-Cream Advanced Consumer Information (Micromedex)
  • Ectosone Regular-Lotion Advanced Consumer Information (Micromedex)
  • Ectosone Scalp Lotion Advanced Consumer Information (Micromedex)
  • Metaderm Mild Advanced Consumer Information (Micromedex)
  • Metaderm Regular Advanced Consumer Information (Micromedex)
  • Novo-Betamet Advanced Consumer Information (Micromedex)
  • Occlucort Advanced Consumer Information (Micromedex)
  • Qualisone Advanced Consumer Information (Micromedex)
  • Betamethasone Topical application Advanced Consumer Information (Micromedex)
  • Betamethasone dipropionate Topical application Advanced Consumer Information (Micromedex)
  • Betamethasone valerate Topical application Advanced Consumer Information (Micromedex)
  • Betamethasone Dipropionate topical AHFS DI Monographs (ASHP)
  • Betamethasone Valerate topical AHFS DI Monographs (ASHP)
  • Betamethasone topical AHFS DI Monographs (ASHP)

Bactroban


Bactroban is a brand name of mupirocin topical, approved by the FDA in the following formulation(s):


BACTROBAN (mupirocin - ointment; topical)



  • Manufacturer: GLAXOSMITHKLINE

    Approval date: December 31, 1987

    Strength(s): 2% [RLD][AB]

BACTROBAN (mupirocin calcium - cream; topical)



  • Manufacturer: GLAXOSMITHKLINE

    Approval date: December 11, 1997

    Strength(s): EQ 2% BASE [RLD]

BACTROBAN (mupirocin calcium - ointment; nasal)



  • Manufacturer: GLAXOSMITHKLINE

    Approval date: September 18, 1995

    Strength(s): EQ 2% BASE [RLD]

Has a generic version of Bactroban been approved?


A generic version of Bactroban has been approved by the FDA. However, this does not mean that the product will necessarily be commercially available - possibly because of drug patents and/or drug exclusivity. The following products are equivalent to Bactroban and have been approved by the FDA:


mupirocin ointment; topical



  • Manufacturer: FOUGERA PHARMS

    Approval date: November 30, 2005

    Strength(s): 2% [AB]


  • Manufacturer: GLENMARK PHARMS

    Approval date: June 8, 2011

    Strength(s): 2% [AB]


  • Manufacturer: PERRIGO NEW YORK

    Approval date: November 7, 2003

    Strength(s): 2% [AB]


  • Manufacturer: TARO

    Approval date: September 23, 2005

    Strength(s): 2% [AB]


  • Manufacturer: TEVA

    Approval date: November 7, 2003

    Strength(s): 2% [AB]

Note: No generic formulation of the following products are available.


  • mupirocin calcium - cream; topical

  • mupirocin calcium - ointment; nasal

Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Bactroban. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents


Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.




  • Pharmaceutical and veterinary compositions of mupirocin and methods for their preparation
    Patent 6,025,389
    Issued: February 15, 2000
    Inventor(s): Zimmerman; Harvey Lee
    Assignee(s): SmithKline Beecham Corporation
    The invention is directed to a pharmaceutical composition comprising a cream base which comprises mupiricin dihydrate, a mineral oil, one or more fatty alcohols or fatty esters, a polyoxyethylene ether or ester surfactant, xanthan gum, water and a method for treating a bacterial infection using said composition.
    Patent expiration dates:

    • October 20, 2014
      ✓ 
      Patent use: TREATMENT OF SECONDARILY INFECTED TRAUMATIC SKIN LESIONS DUE TO S. AUREUS AND S. PYOGENES
      ✓ 
      Drug product



See also...

  • Bactroban Consumer Information (Drugs.com)
  • Bactroban Cream Consumer Information (Wolters Kluwer)
  • Bactroban Ointment Consumer Information (Wolters Kluwer)
  • Bactroban Consumer Information (Cerner Multum)
  • Bactroban Nasal Advanced Consumer Information (Micromedex)
  • Bactroban Topical Advanced Consumer Information (Micromedex)
  • Mupirocin Cream Consumer Information (Wolters Kluwer)
  • Mupirocin Ointment Consumer Information (Wolters Kluwer)
  • Mupirocin nasal Consumer Information (Cerner Multum)
  • Mupirocin topical Consumer Information (Cerner Multum)
  • Mupirocin Nasal Advanced Consumer Information (Micromedex)
  • Mupirocin Topical Advanced Consumer Information (Micromedex)
  • Mupirocin AHFS DI Monographs (ASHP)

Xalkori


Xalkori is a brand name of crizotinib, approved by the FDA in the following formulation(s):


XALKORI (crizotinib - capsule; oral)



  • Manufacturer: PFIZER

    Approval date: August 26, 2011

    Strength(s): 200MG, 250MG [RLD]

Has a generic version of Xalkori been approved?


No. There is currently no therapeutically equivalent version of Xalkori available.


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Xalkori. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents


Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.




  • Aminoheteroaryl compounds as protein kinase inhibitors
    Patent 7,230,098
    Issued: June 12, 2007
    Inventor(s): Cui; Jingrong Jean & Bhumralkar; Dilip & Botrous; Iriny & Chu; Ji Yu & Funk; Lee A. & Hanau; Cathleen Elizabeth & Harris; G. Davis & Jia; Lei & Johnson; Joanne & Kolodziej; Stephen A. & Kung; Pei-Pei & Li; Xiaoyuan (Sharon) & Lin; Jason (Qishen) & Meng; Jerry Jialun & Nambu; Mitchel
    Assignee(s): Sugen, Inc.
    Aminopyridine and aminopyrazine compounds of formula (1), compositions including these compounds, and methods of their use are provided. Preferred compounds of formula 1 have activity as protein kinase inhibitors, including as inhibitors of c-MET
    Patent expiration dates:

    • March 1, 2025
      ✓ 
      Drug substance




  • Method of treating abnormal cell growth
    Patent 7,825,137
    Issued: November 2, 2010
    Inventor(s): Christensen; James Gail & Zou; Yahong
    Assignee(s): Pfizer Inc.
    The present invention relates to the use of (R)-3-[1-(2,6-Dichloro-3-fluoro-phenyl)-ethoxy]-5-(1-piperidin-4-yl-1H-pyrazol-4-yl)-pyridin-2-ylamine, a novel c-Met/HGFR inhibitor, for treating abnormal cell growth in mammals. In particular, the invention provides methods of treating mammals suffering from cancer.
    Patent expiration dates:

    • May 12, 2027
      ✓ 
      Patent use: TREATMENT OF A CANCER MEDIATED BY AN ANAPLASTIC LYMPHOMA KINASE (ALK)




  • Enantiomerically pure aminoheteroaryl compounds as protein kinase inhibitors
    Patent 7,858,643
    Issued: December 28, 2010
    Inventor(s): Cui; Jingrong Jean & Funk; Lee Andrew & Jia; Lei & Kung; Pei-Pei & Meng; Jerry Jialun & Nambu; Mitchell David & Pairish; Mason Alan & Shen; Hong & Tran-Dube; Michelle
    Assignee(s): Agouron Pharmaceuticals, Inc.
    Enantiomerically pure compound of formula 1 are provided, as well as methods for their synthesis and use. Preferred compounds are potent inhibitors of the c-Met protein kinase, and are useful in the treatment of abnormal cell growth disorders, such as cancers.
    Patent expiration dates:

    • October 8, 2029
      ✓ 
      Drug substance
      ✓ 
      Drug product



Related Exclusivities

Exclusivity is exclusive marketing rights granted by the FDA upon approval of a drug and can run concurrently with a patent or not. Exclusivity is a statutory provision and is granted to an NDA applicant if statutory requirements are met.

  • Exclusivity expiration dates:
    • August 26, 2016 - NEW CHEMICAL ENTITY

    • August 26, 2018 - ORPHAN DRUG EXCLUSIVITY

See also...

  • Xalkori Consumer Information (Drugs.com)
  • Xalkori Consumer Information (Wolters Kluwer)
  • Xalkori Consumer Information (Cerner Multum)
  • Crizotinib Consumer Information (Wolters Kluwer)
  • Crizotinib Consumer Information (Cerner Multum)

Baraclude


Baraclude is a brand name of entecavir, approved by the FDA in the following formulation(s):


BARACLUDE (entecavir - solution; oral)



  • Manufacturer: BRISTOL MYERS SQUIBB

    Approval date: March 29, 2005

    Strength(s): 0.05MG/ML [RLD]

BARACLUDE (entecavir - tablet; oral)



  • Manufacturer: BRISTOL MYERS SQUIBB

    Approval date: March 29, 2005

    Strength(s): 0.5MG, 1MG [RLD]

Has a generic version of Baraclude been approved?


No. There is currently no therapeutically equivalent version of Baraclude available.


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Baraclude. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents


Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.




  • Hydroxymethyl (methylenecyclopentyl) purines and pyrimidines
    Patent 5,206,244
    Issued: April 27, 1993
    Inventor(s): Zahler; Robert & Slusarchyk; William A.
    Assignee(s): E. R. Squibb & Sons, Inc.
    Antiviral activity is exhibited by compounds having the formula ##STR1## and its pharmaceutically acceptable salts.
    Patent expiration dates:

    • February 21, 2015
      ✓ 
      Drug substance



Related Exclusivities

Exclusivity is exclusive marketing rights granted by the FDA upon approval of a drug and can run concurrently with a patent or not. Exclusivity is a statutory provision and is granted to an NDA applicant if statutory requirements are met.

  • Exclusivity expiration dates:
    • October 15, 2013 - DOSING REGIMEN FOR ADULT PATIENTS WITH CHRONIC HEPATITIS B (CHB) AND DECOMPENSATED LIVER DESEASE

See also...

  • Baraclude Consumer Information (Drugs.com)
  • Baraclude Consumer Information (Wolters Kluwer)
  • Baraclude Solution Consumer Information (Wolters Kluwer)
  • Baraclude Consumer Information (Cerner Multum)
  • Baraclude Advanced Consumer Information (Micromedex)
  • Baraclude AHFS DI Monographs (ASHP)
  • Entecavir Consumer Information (Wolters Kluwer)
  • Entecavir Solution Consumer Information (Wolters Kluwer)
  • Entecavir Consumer Information (Cerner Multum)
  • Entecavir Advanced Consumer Information (Micromedex)
  • Entecavir AHFS DI Monographs (ASHP)

NuvaRing


NuvaRing is a brand name of ethinyl estradiol/etonogestrel, approved by the FDA in the following formulation(s):


NUVARING (ethinyl estradiol; etonogestrel - ring; vaginal)



  • Manufacturer: ORGANON USA INC

    Approval date: October 3, 2001

    Strength(s): 0.015MG;0.12MG [RLD]

Has a generic version of NuvaRing been approved?


No. There is currently no therapeutically equivalent version of NuvaRing available.


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of NuvaRing. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents


Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.




  • Drug delivery system for two or more active substances
    Patent 5,989,581
    Issued: November 23, 1999
    Inventor(s): Groenewegen; Rudolf Johannes Joseph
    Assignee(s): Akzo Nobel N.V.
    The present invention is dealing with a drug delivery system, preferably in a ring-shaped form suitable for vaginal administration, for the simultaneous release of a progestogenic steroid compound and an estrogenic steroid compound in a fixed physiological ratio over a prolonged period of time. The drug delivery system comprises at least one compartment comprising a thermoplastic polymer core containing the mixture of the progestogenic and estrogenic compounds and a thermoplastic polymer skin, the progestogenic compound being initially dissolved in the polymer core material in a relatively low degree of supersaturation.
    Patent expiration dates:

    • April 8, 2018



See also...

  • NuvaRing Consumer Information (Drugs.com)
  • NuvaRing Ring Consumer Information (Wolters Kluwer)
  • NuvaRing Consumer Information (Cerner Multum)
  • NuvaRing Advanced Consumer Information (Micromedex)
  • Etonogestrel/Ethinyl Estradiol Ring Consumer Information (Wolters Kluwer)
  • Ethinyl estradiol and etonogestrel Consumer Information (Cerner Multum)
  • Ethinyl estradiol and etonogestrel Vaginal Advanced Consumer Information (Micromedex)

Xolegel


Xolegel is a brand name of ketoconazole topical, approved by the FDA in the following formulation(s):


XOLEGEL (ketoconazole - gel; topical)



  • Manufacturer: AQUA PHARMS

    Approval date: July 28, 2006

    Strength(s): 2% [RLD]

Has a generic version of Xolegel been approved?


No. There is currently no therapeutically equivalent version of Xolegel available.


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Xolegel. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents


Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.




  • Anhydrous topical skin preparations
    Patent 7,179,475
    Issued: February 20, 2007
    Inventor(s): Burnett; Katherine M. & Kurtz; Ellen S.
    Assignee(s): Johnson & Johnson Consumer Companies, Inc.
    The present invention provides anhydrous compositions for topical delivery of a medicament comprising (A) a penetration enhancer/solvent selected from the group consisting of alcohol, propylene glycol, or a combination thereof; (B) a humectant/solvent selected from the group consisting of polyethylene glycol, glycerin, sorbitol, xylitol, or any combination of any of the foregoing; and (C) an anhydrous vehicle. In an alternate embodiment, the present invention provides anhydrous compositions for topical delivery of a medicament which comprise (A) a penetration enhancer/solvent selected from the group consisting of alcohol, propylene glycol, or a combination thereof; (B) a humectant/solvent selected from the group consisting of polyethylene glycol, glycerin, sorbitol, xylitol or any combination of any of the foregoing; (C) an anhydrous vehicle; and (D) a medicament. Also provided are methods for topically delivering a medicament to an animal, such as a mammal or a human patient, in need of the medicament by topically administering to the animal the compositions of the present invention.
    Patent expiration dates:

    • December 4, 2018
      ✓ 
      Patent use: TREATMENT OF SEBORRHEA DERMATITIS IN HUMANS
      ✓ 
      Drug product



See also...

  • Xolegel Consumer Information (Drugs.com)
  • Xolegel Gel Consumer Information (Wolters Kluwer)
  • Xolegel Consumer Information (Cerner Multum)
  • Xolegel Topical Advanced Consumer Information (Micromedex)
  • Ketoconazole Cream Consumer Information (Wolters Kluwer)
  • Ketoconazole Foam Consumer Information (Wolters Kluwer)
  • Ketoconazole Gel Consumer Information (Wolters Kluwer)
  • Ketoconazole Shampoo Consumer Information (Wolters Kluwer)
  • Ketoconazole topical Consumer Information (Cerner Multum)
  • Ketoderm Topical Advanced Consumer Information (Micromedex)
  • Ketoconazole Topical Advanced Consumer Information (Micromedex)
  • Ketoconazole topical AHFS DI Monographs (ASHP)

Xyzal


Xyzal is a brand name of levocetirizine, approved by the FDA in the following formulation(s):


XYZAL (levocetirizine dihydrochloride - solution; oral)



  • Manufacturer: UCB INC

    Approval date: January 28, 2008

    Strength(s): 2.5MG/5ML [RLD][AA]

XYZAL (levocetirizine dihydrochloride - tablet; oral)



  • Manufacturer: UCB INC

    Approval date: May 25, 2007

    Strength(s): 5MG [RLD][AB]

Has a generic version of Xyzal been approved?


A generic version of Xyzal has been approved by the FDA. However, this does not mean that the product will necessarily be commercially available - possibly because of drug patents and/or drug exclusivity. The following products are equivalent to Xyzal and have been approved by the FDA:


levocetirizine dihydrochloride solution; oral



  • Manufacturer: SYNTHON PHARMS

    Approval date: November 7, 2011

    Strength(s): 2.5MG/5ML [AA]

levocetirizine dihydrochloride tablet; oral



  • Manufacturer: DR REDDYS LABS LTD

    Approval date: February 24, 2011

    Strength(s): 5MG [AB]


  • Manufacturer: GLENMARK GENERICS

    Approval date: February 24, 2011

    Strength(s): 5MG [AB]


  • Manufacturer: SYNTHON PHARMS

    Approval date: November 26, 2010

    Strength(s): 5MG [AB]


  • Manufacturer: TEVA PHARMS

    Approval date: August 22, 2011

    Strength(s): 5MG [AB]

Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Xyzal. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents


Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.




  • Methods for treating allergic disorders using optically pure (-) cetirizine
    Patent 5,698,558
    Issued: December 16, 1997
    Inventor(s): Gray; Nancy M.
    Assignee(s): Sepracor, Inc.
    Methods are disclosed utilizing optically pure (-) cetirizine for the treatment of seasonal and perennial allergic rhinitis in humans while avoiding the concomitant liability of adverse effects associated with the racemic mixture of cetirizine. The optically pure (-) isomer is also useful for the treatment of allergic asthma.
    Patent expiration dates:

    • September 24, 2012
      ✓ 
      Patent use: RELIEF OF SYMPTOMS ASSOCIATED WITH SEASONAL AND PERENNIAL ALLERGIC RHINITIS


    • September 24, 2012
      ✓ 
      Patent use: RELIEF OF SYMPTOMS ASSOCIATED WITH SEASONAL AND PERENNIAL ALLERGIC RHINITIS


    • March 24, 2013
      ✓ 
      Pediatric exclusivity



Related Exclusivities

Exclusivity is exclusive marketing rights granted by the FDA upon approval of a drug and can run concurrently with a patent or not. Exclusivity is a statutory provision and is granted to an NDA applicant if statutory requirements are met.

  • Exclusivity expiration dates:
    • November 25, 2010 - PEDIATRIC EXCLUSIVITY

    • August 21, 2012 - NEW PATIENT POPULATION

    • February 21, 2013 - PEDIATRIC EXCLUSIVITY

See also...

  • Xyzal Consumer Information (Drugs.com)
  • Xyzal Consumer Information (Wolters Kluwer)
  • Xyzal Solution Consumer Information (Wolters Kluwer)
  • Xyzal Consumer Information (Cerner Multum)
  • Xyzal Advanced Consumer Information (Micromedex)
  • Xyzal AHFS DI Monographs (ASHP)
  • Levocetirizine Consumer Information (Wolters Kluwer)
  • Levocetirizine Solution Consumer Information (Wolters Kluwer)
  • Levocetirizine Consumer Information (Cerner Multum)
  • Levocetirizine Advanced Consumer Information (Micromedex)
  • Levocetirizine Dihydrochloride AHFS DI Monographs (ASHP)

Xyrem


Xyrem is a brand name of sodium oxybate, approved by the FDA in the following formulation(s):


XYREM (sodium oxybate - solution; oral)



  • Manufacturer: JAZZ

    Approval date: July 17, 2002

    Strength(s): 500MG/ML [RLD]

Has a generic version of Xyrem been approved?


No. There is currently no therapeutically equivalent version of Xyrem available.


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Xyrem. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents


Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.




  • Microbiologically sound and stable solutions of gamma-hydroxybutyrate salt for the treatment of narcolepsy
    Patent 6,780,889
    Issued: August 24, 2004
    Inventor(s): Harry; Cook & Martha; Hamilton & Douglas; Danielson & Colette; Goderstad & Dayton; Reardan
    Assignee(s): Orphan Medical, Inc.
    Disclosed are formulations of gamma-hydroxybutyrate in an aqueous medium that are resistant to microbial growth. Also disclosed are formulations of gamma-hydroxybutyrate that are also resistant to the conversion into GBL. Disclosed are methods to treat sleep disorders, including narcolepsy, with these stable formulations of GHB. The present invention also provides methods to treat alcohol and opiate withdrawal, reduced levels of growth hormone, increased intracranial pressure, and physical pain in a patient.
    Patent expiration dates:

    • July 4, 2020
      ✓ 
      Drug product




  • Microbiologically sound and stable solutions of gamma-hydroxybutyrate salt for the treatment of narcolepsy
    Patent 7,262,219
    Issued: August 28, 2007
    Inventor(s): Cook; Harry & Hamilton; Martha & Danielson; Douglas & Goderstad; Colette & Reardan; Dayton
    Assignee(s): Orphan Medical, Inc.
    Disclosed are formulations of gamma-hydroxybutyrate in an aqueous medium that are resistant to microbial growth. Also disclosed are formulations of gamma-hydroxybutyrate that are also resistant to the conversion into GBL. Disclosed are methods to treat sleep disorders, including narcolepsy, with these stable formulations of GHB. The present invention also provides methods to treat alcohol and opiate withdrawal, reduced levels of growth hormone, increased intracranial pressure, and physical pain in a patient.
    Patent expiration dates:

    • July 4, 2020
      ✓ 
      Drug product




  • Sensitive drug distribution system and method
    Patent 7,668,730
    Issued: February 23, 2010
    Inventor(s): Reardan; Dayton T. & Engle; Patti & Gagne; Bob
    Assignee(s): JPI Commercial, LLC.
    A drug distribution system and method utilizes a central pharmacy and database to track all prescriptions for a sensitive drug. Information is kept in the database regarding all physicians allowed to prescribe the sensitive drug, and all patients receiving the drug. Abuses are identified by monitoring data in the database for prescription patterns by physicians and prescriptions obtained by patients. Further verification is made that the physician is eligible to prescribe the drug by consulting a separate database, and optionally whether any actions are taken against the physician. Multiple controls beyond those for normal drugs are imposed on the distribution depending on the sensitivity of the drug.
    Patent expiration dates:

    • June 16, 2024
      ✓ 
      Patent use: METHOD OF TREATING A PATIENT WITH A PRESCRIPTION DRUG USING A COMPUTER DATABASE IN A COMPUTER SYSTEM FOR DISTRIBUTION




  • Sensitive drug distribution system and method
    Patent 7,765,106
    Issued: July 27, 2010
    Inventor(s): Reardan; Dayton T. & Engel; Patti A. & Gagne; Bob
    Assignee(s): JPI Commercial, LLC
    A drug distribution system and method utilizes a central pharmacy and database to track all prescriptions for a sensitive drug. Information is kept in the database regarding all physicians allowed to prescribe the sensitive drug, and all patients receiving the drug. Abuses are identified by monitoring data in the database for prescription patterns by physicians and prescriptions obtained by patients. Further verification is made that the physician is eligible to prescribe the drug by consulting a separate database, and optionally whether any actions are taken against the physician. Multiple controls beyond those for normal drugs are imposed on the distribution depending on the sensitivity of the drug.
    Patent expiration dates:

    • June 16, 2024
      ✓ 
      Patent use: A METHOD OF TREATING A PATIENT WITH A PRESCRIPTION DRUG USING AN EXCLUSIVE COMPUTER DATABASE IN A COMPUTER SYSTEM FOR DISTRIBUTION




  • Sensitive drug distribution system and method
    Patent 7,765,107
    Issued: July 27, 2010
    Inventor(s): Reardan; Dayton T. & Engel; Patti A. & Gagne; Bob
    Assignee(s): JPI Commercial, LLC.
    A drug distribution system and method utilizes a central pharmacy and database to track all prescriptions for a sensitive drug. Information is kept in the database regarding all physicians allowed to prescribe the sensitive drug, and all patients receiving the drug. Abuses are identified by monitoring data in the database for prescription patterns by physicians and prescriptions obtained by patients. Further verification is made that the physician is eligible to prescribe the drug by consulting a separate database, and optionally whether any actions are taken against the physician. Multiple controls beyond those for normal drugs are imposed on the distribution depending on the sensitivity of the drug.
    Patent expiration dates:

    • June 16, 2024
      ✓ 
      Patent use: A METHOD TO CONTROL ABUSE OF A SENSITIVE DRUG BY CONTROLLING WITH A COMPUTER PROCESSOR THE DISTRIBUTION OF THE SENSITIVE DRUG VIA AN EXCLUSIVITY CENTRAL PHARMACY THAT MAINTAINS A CENTRAL DATABASE




  • Microbiologically sound and stable solutions of gamma-hydroxybutyrate salt for the treatment of narcolepsy
    Patent 7,851,506
    Issued: December 14, 2010
    Inventor(s): Cook; Harry & Hamilton; Martha & Danielson; Douglas & Goderstad; Colette & Reardan; Dayton
    Assignee(s): Jazz Pharmaceuticals, Inc.
    Disclosed are formulations of gamma-hydroxybutyrate in an aqueous medium that are resistant to microbial growth. Also disclosed are formulations of gamma-hydroxybutyrate that are also resistant to the conversion into GBL. Disclosed are methods to treat sleep disorders, including narcolepsy, with these stable formulations of GHB. The present invention also provides methods to treat alcohol and opiate withdrawal, reduced levels of growth hormone, increased intracranial pressure, and physical pain in a patient.
    Patent expiration dates:

    • December 22, 2019
      ✓ 
      Patent use: METHOD OF TREATING CATAPLEXY IN PATIENTS WITH NARCOLEPSY


    • December 22, 2019
      ✓ 
      Patent use: METHOD OF TREATING EXCESSIVE DAYTIME SLEEPINESS IN PATIENTS WITH NARCOLEPSY




  • Sensitive drug distribution system and method
    Patent 7,895,059
    Issued: February 22, 2011
    Inventor(s): Reardan; Dayton T. & Engel; Patti A. & Gagne; Bob
    Assignee(s): Jazz Pharmaceuticals, Inc.
    A drug distribution system and method utilizes a central pharmacy and database to track all prescriptions for a sensitive drug. Information is kept in the database regarding all physicians allowed to prescribe the sensitive drug, and all patients receiving the drug. Abuses are identified by monitoring data in the database for prescription patterns by physicians and prescriptions obtained by patients. Further verification is made that the physician is eligible to prescribe the drug by consulting a separate database, and optionally whether any actions are taken against the physician. Multiple controls beyond those for normal drugs are imposed on the distribution depending on the sensitivity of the drug.
    Patent expiration dates:

    • December 17, 2022
      ✓ 
      Patent use: METHOD OF TREATING A PATIENT WITH A PRESCRIPTION DRUG USING A COMPUTER DATABASE IN A COMPUTER SYSTEM FOR DISTRIBUTION



Related Exclusivities

Exclusivity is exclusive marketing rights granted by the FDA upon approval of a drug and can run concurrently with a patent or not. Exclusivity is a statutory provision and is granted to an NDA applicant if statutory requirements are met.

  • Exclusivity expiration dates:
    • November 18, 2012 - ORPHAN DRUG EXCLUSIVITY

See also...

  • Xyrem Consumer Information (Drugs.com)
  • Xyrem Consumer Information (Cerner Multum)
  • Xyrem Advanced Consumer Information (Micromedex)
  • Xyrem AHFS DI Monographs (ASHP)
  • Sodium oxybate Consumer Information (Cerner Multum)
  • Sodium oxybate Advanced Consumer Information (Micromedex)
  • Sodium Oxybate AHFS DI Monographs (ASHP)

Xanax


See also: Generic Xanax XR


Xanax is a brand name of alprazolam, approved by the FDA in the following formulation(s):


XANAX (alprazolam - tablet; oral)



  • Manufacturer: PHARMACIA AND UPJOHN

    Approved Prior to Jan 1, 1982

    Strength(s): 0.25MG [AB], 0.5MG [AB], 1MG [RLD][AB]


  • Manufacturer: PHARMACIA AND UPJOHN

    Approval date: November 27, 1985

    Strength(s): 2MG [AB]

Has a generic version of Xanax been approved?


Yes. The following products are equivalent to Xanax:


alprazolam tablet; oral



  • Manufacturer: ACTAVIS ELIZABETH

    Approval date: October 31, 1993

    Strength(s): 0.25MG [AB], 0.5MG [AB], 1MG [AB], 2MG [AB]


  • Manufacturer: ALPHAPHARM

    Approval date: October 19, 1993

    Strength(s): 0.25MG [AB], 0.5MG [AB], 1MG [AB]


  • Manufacturer: ALPHAPHARM

    Approval date: May 7, 1997

    Strength(s): 2MG [AB]


  • Manufacturer: APOTEX INC

    Approval date: January 19, 2007

    Strength(s): 0.25MG [AB], 0.5MG [AB], 1MG [AB], 2MG [AB]


  • Manufacturer: BOCA PHARMA

    Approval date: September 17, 2010

    Strength(s): 0.25MG [AB], 0.5MG [AB], 1MG [AB], 2MG [AB]


  • Manufacturer: DAVA INTL INC

    Approval date: October 19, 1993

    Strength(s): 0.25MG [AB], 0.5MG [AB], 1MG [AB], 2MG [AB]


  • Manufacturer: MYLAN

    Approval date: January 27, 1994

    Strength(s): 0.25MG [AB], 0.5MG [AB], 1MG [AB], 2MG [AB]


  • Manufacturer: SANDOZ

    Approval date: December 29, 1995

    Strength(s): 0.25MG [AB], 0.5MG [AB], 1MG [AB]


  • Manufacturer: SANDOZ

    Approval date: March 25, 1998

    Strength(s): 2MG [AB]


  • Manufacturer: SUN PHARMA GLOBAL

    Approval date: June 17, 2010

    Strength(s): 0.25MG [AB], 0.5MG [AB], 1MG [AB], 2MG [AB]


  • Manufacturer: VINTAGE

    Approval date: September 25, 2008

    Strength(s): 0.25MG [AB], 0.5MG [AB], 1MG [AB]


  • Manufacturer: VINTAGE

    Approval date: December 12, 2008

    Strength(s): 2MG [AB]

Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Xanax. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents

There are no current U.S. patents associated with Xanax.

See also...

  • Xanax Consumer Information (Drugs.com)
  • Xanax Consumer Information (Wolters Kluwer)
  • Xanax Consumer Information (Cerner Multum)
  • Xanax Advanced Consumer Information (Micromedex)
  • Alprazolam Consumer Information (Drugs.com)
  • Alprazolam Consumer Information (Wolters Kluwer)
  • Alprazolam Extended-Release Tablets Consumer Information (Wolters Kluwer)
  • Alprazolam Orally Disintegrating Tablets Consumer Information (Wolters Kluwer)
  • Alprazolam Solution Consumer Information (Wolters Kluwer)
  • Alprazolam Consumer Information (Cerner Multum)
  • Alti-Alprazolam Advanced Consumer Information (Micromedex)
  • Gabazolamine-0.5 Advanced Consumer Information (Micromedex)
  • Alprazolam Advanced Consumer Information (Micromedex)
  • Alprazolam AHFS DI Monographs (ASHP)

Xopenex HFA


See also: Generic Xopenex


Xopenex HFA is a brand name of levalbuterol, approved by the FDA in the following formulation(s):


XOPENEX HFA (levalbuterol tartrate - aerosol, metered; inhalation)



  • Manufacturer: SUNOVION

    Approval date: March 11, 2005

    Strength(s): EQ 0.045MG BASE/INH [RLD]

Has a generic version of Xopenex HFA been approved?


No. There is currently no therapeutically equivalent version of Xopenex HFA available.


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Xopenex HFA. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents


Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.




  • Method for treating asthma using optically pure (R)-albuterol
    Patent 5,362,755
    Issued: November 8, 1994
    Inventor(s): Barberich; Timothy J. & Young; James W.
    Assignee(s): Sepracor, Inc.
    The optically pure R(-) isomer of albuterol, which is substantially free of the S(+) isomer, is a potent bronchodilator for relieving the symptoms associated with asthma in individuals. A method is disclosed utilizing the optically pure R(-) isomer of albuterol for treating asthma while minimizing the side effects associated with chronic administration of racemic albuterol.
    Patent expiration dates:

    • March 25, 2013
      ✓ 
      Patent use: TREATMENT OR PREVENTION OF BRONCHOSPASM OR ASTHMATIC SYMPTOMS




  • Method for treating asthma using optically pure R(-) albuterol
    Patent 5,547,994
    Issued: August 20, 1996
    Inventor(s): Barberich; Timothy J. & Young; James W.
    Assignee(s): Sepracor, Inc.
    The optically pure R(-) isomer of albuterol, which is substantially free of the S(+) isomer, is a potent bronchodilator for relieving the symptoms associated with asthma in individuals. A method is disclosed utilizing the optically pure R(-) isomer of albuterol for treating asthma while minimizing the side effects associated with albuterol.
    Patent expiration dates:

    • August 20, 2013
      ✓ 
      Patent use: TREATMENT OR PREVENTION OF BRONCHOSPASM OR ASTHMATIC SYMPTOMS




  • Medicinal aerosol formulations
    Patent 5,605,674
    Issued: February 25, 1997
    Inventor(s): Purewal; Tarlochan S. & Greenleaf; David J.
    Assignee(s): Riker Laboratories, Inc.
    A self-propelling aerosol formulation which may be free from CFC's which comprises a medicament, 1,1,1,2-tetrafluoroethane, a surface active agent and at least one compound having a higher polarity than 1,1,1,2-tetrafluoroethane.
    Patent expiration dates:

    • February 25, 2014
      ✓ 
      Drug product




  • Seals for use in an aerosol delivery device
    Patent 5,836,299
    Issued: November 17, 1998
    Inventor(s): Kwon; Oh-Seung
    Assignee(s): Minnesota Mining & Manufacturing Co.
    A device for delivering an aerosol, comprising: a casing member, a valve stem, and a diaphragm. The diaphragm is made of an ethylene-propylene-diene rubber ("EPDM") and is stable to dimensional change when exposed to 1,1,1,2-tetrafluoroethane or 1,1,1,2,3,3,3-heptafluoroethane.
    Patent expiration dates:

    • November 17, 2015
      ✓ 
      Drug product




  • Levalbuterol salt
    Patent 7,256,310
    Issued: August 14, 2007
    Inventor(s): McGlynn; Paul & Bakale; Roger & Sturge; Craig
    Assignee(s): Sepracor Inc.
    Levalbuterol L-tartrate affords crystals possessing properties desirable for use in a metered dose inhaler.
    Patent expiration dates:

    • October 8, 2024
      ✓ 
      Patent use: TREATMENT OR PREVENTION OF BRONCHOSPASM OR ASTHMATIC SYMPTOMS
      ✓ 
      Drug substance
      ✓ 
      Drug product



See also...

  • Xopenex HFA Aerosol Consumer Information (Wolters Kluwer)
  • Xopenex HFA Consumer Information (Cerner Multum)
  • Xopenex HFA Advanced Consumer Information (Micromedex)
  • Levalbuterol Aerosol Consumer Information (Wolters Kluwer)
  • Levalbuterol Solution Consumer Information (Wolters Kluwer)
  • Levalbuterol Consumer Information (Cerner Multum)
  • Xopenex Pediatric Advanced Consumer Information (Micromedex)
  • Levalbuterol Inhalation, oral/nebulization Advanced Consumer Information (Micromedex)
  • Levalbuterol AHFS DI Monographs (ASHP)

Xarelto


Xarelto is a brand name of rivaroxaban, approved by the FDA in the following formulation(s):


XARELTO (rivaroxaban - tablet; oral)



  • Manufacturer: JANSSEN PHARMS

    Approval date: July 1, 2011

    Strength(s): 10MG [RLD]


  • Manufacturer: JANSSEN PHARMS

    Approval date: November 4, 2011

    Strength(s): 15MG, 20MG [RLD]

Has a generic version of Xarelto been approved?


No. There is currently no therapeutically equivalent version of Xarelto available.


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Xarelto. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents


Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.




  • Substituted oxazolidinones and their use in the field of blood coagulation
    Patent 7,157,456
    Issued: January 2, 2007
    Inventor(s): Straub; Alexander & Lampe; Thomas & Pohlmann; Jens & Röhrig; Susanne & Perzborn; Elisabeth & Schlemmer; Karl-Heinz & Pernerstorfer; Joseph
    Assignee(s): Bayer HealthCare AG
    The invention relates to the field of blood coagulation. Novel oxazolidinone derivatives of the general formula (I) processes for their preparation and their use as medicinally active compounds for the prophylaxis and/or treatment of disorders are described.
    Patent expiration dates:

    • February 8, 2021
      ✓ 
      Drug substance
      ✓ 
      Drug product




  • Substituted oxazolidinones and their use in the field of blood coagulation
    Patent 7,585,860
    Issued: September 8, 2009
    Inventor(s): Straub; Alexander & Lampe; Thomas & Pohlmann; Jens & Rohrig; Susanne & Perzborn; Elisabeth & Schlemmer; Karl-Heinz & Pernerstorfer; Joseph
    Assignee(s): Bayer Schering Pharma Aktiengesellschaft
    The invention relates to the field of blood coagulation. Novel oxazolidinone derivatives of the general formula (I) processes for their preparation and their use as medicinally active compounds for the prophylaxis and/or treatment of disorders are described.
    Patent expiration dates:

    • December 11, 2020
      ✓ 
      Drug substance




  • Substituted oxazolidinones and their use in the field of blood coagulation
    Patent 7,592,339
    Issued: September 22, 2009
    Inventor(s): Straub; Alexander & Lampe; Thomas & Pohlmann; Jens & Rohrig; Susanne & Perzborn; Elisabeth & Schlemmer; Karl-Heinz & Pernerstorfer; Joseph
    Assignee(s): Bayer Schering Pharma Aktiengesellschaft
    The invention relates to the field of blood coagulation. Novel oxazolidinone derivatives of the general formula (I) processes for their preparation and their use as medicinally active compounds for the prophylaxis and/or treatment of disorders are described.
    Patent expiration dates:

    • December 11, 2020
      ✓ 
      Patent use: PROPHYLAXIS OF DEEP VEIN THROMBOSIS (DVT)


    • December 11, 2020
      ✓ 
      Patent use: REDUCING THE RISK OF STROKE AND SYSTEMIC EMBOLISM



Related Exclusivities

Exclusivity is exclusive marketing rights granted by the FDA upon approval of a drug and can run concurrently with a patent or not. Exclusivity is a statutory provision and is granted to an NDA applicant if statutory requirements are met.

  • Exclusivity expiration dates:
    • November 4, 2014 - REDUCE THE RISK OF STROKE AND SYSTEMIC EMBOLISM IN PATIENTS WITH NONVALVULAR ATRIAL FIBRILLATION.

    • July 1, 2016 - NEW CHEMICAL ENTITY

See also...

  • Xarelto Consumer Information (Drugs.com)
  • Xarelto Consumer Information (Wolters Kluwer)
  • Xarelto Consumer Information (Cerner Multum)
  • Xarelto Advanced Consumer Information (Micromedex)
  • Rivaroxaban Consumer Information (Wolters Kluwer)
  • Rivaroxaban Consumer Information (Cerner Multum)
  • Rivaroxaban Advanced Consumer Information (Micromedex)

Welchol


Welchol is a brand name of colesevelam, approved by the FDA in the following formulation(s):


WELCHOL (colesevelam hydrochloride - for suspension; oral)



  • Manufacturer: DAIICHI SANKYO

    Approval date: October 2, 2009

    Strength(s): 1.875GM/PACKET, 3.75GM/PACKET [RLD]

WELCHOL (colesevelam hydrochloride - tablet; oral)



  • Manufacturer: DAIICHI SANKYO

    Approval date: May 26, 2000

    Strength(s): 625MG [RLD]

Has a generic version of Welchol been approved?


No. There is currently no therapeutically equivalent version of Welchol available.


Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Welchol. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.

See also: About generic drugs.




Related Patents


Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.




  • Amine polymer sequestrant and method of cholesterol depletion
    Patent 5,607,669
    Issued: March 4, 1997
    Inventor(s): Mandeville, III; W. Harry & Holmes-Farley; Stephen R.
    Assignee(s): GelTex Pharmaceuticals, Inc.
    An amine polymer includes first and second substituents bound to amines of the polymer. The first substituent includes a hydrophobic moiety. The second substituent includes a quaternary amine-containing moiety. A method for binding bile salts of bile acids in a mammal includes orally administering to the mammal a therapeutically-effective amount of the amine polymer.
    Patent expiration dates:

    • June 10, 2014
      ✓ 
      Patent use: USE AS A BILE ACID SEQUESTRANT


    • June 10, 2014
      ✓ 
      Patent use: USE AS A BILE ACID SEQUESTRANT FOR LOWERING CHOLESTEROL


    • December 10, 2014
      ✓ 
      Pediatric exclusivity




  • Method for removing bile salts from a patient with alkylated amine polymers
    Patent 5,679,717
    Issued: October 21, 1997
    Inventor(s): Mandeville, III; W. Harry & Holmes-Farley; Stephen Randall
    Assignee(s): GelTex Pharmaceuticals, Inc.
    A method for removing bile salts from a patient that includes administering to the patient a therapeutically effective amount of product produced by a process comprising alkylating one or more crosslinked amine polymers, salts or copolymers thereof with at least one alkylating agent. The reaction product is characterized in that: (i) at least some of the nitrogen atoms are unreacted with alkylating agent; and (ii) less than 10 mol% of the nitrogen atoms in the polymer react with the alkylating agent to form quaternary ammonium units.
    Patent expiration dates:

    • April 29, 2014
      ✓ 
      Patent use: USE AS A BILE ACID SEQUESTRANT


    • April 29, 2014
      ✓ 
      Patent use: USE AS A BILE ACID SEQUESTRANT FOR LOWERING CHOLESTEROL


    • October 29, 2014
      ✓ 
      Pediatric exclusivity




  • Alkylated amine polymers
    Patent 5,693,675
    Issued: December 2, 1997
    Inventor(s): Mandeville, III; W. Harry & Holmes-Farley; Stephen Randall
    Assignee(s): GelTex Pharmaceuticals Inc.
    The invention relates to alkylated amine polymers and a method for removing bile salts from a patient that includes administering to the patient a therapeutically effective amount of product produced by a process comprising alkylating one or more crosslinked amine polymers, salts or copolymers thereof with at least one alkylating agent. The reaction product is characterized in that: (i) at least some of the nitrogen atoms are unreacted with alkylating agent; and (ii) less than 10 mol % of the nitrogen atoms in the polymer react with the alkylating agent to form quaternary ammonium units.
    Patent expiration dates:

    • December 2, 2014


    • December 2, 2014
      ✓ 
      Drug substance


    • June 2, 2015
      ✓ 
      Pediatric exclusivity




  • Process for removing bile salts from a patient and alkylated compositions therefor
    Patent 5,917,007
    Issued: June 29, 1999
    Inventor(s): Mandeville, III; W. Harry & Holmes-Farley; Stephen Randall
    Assignee(s): GelTex Pharmaceuticals, Inc.
    The invention relates to a method for removing bile salts from a patient in need thereof and compositions useful in the method. The method comprises administering to the patient a therapeutically effective amount of an alkylated and crosslinked polymer. The alkylated and crosslinked polymer comprises the reaction product of polymers, or salts and copolymers thereof having amine containing repeat units, with at least one aliphatic alkylating agent and a crosslinking agent.
    Patent expiration dates:

    • April 29, 2014
      ✓ 
      Patent use: USE AS A BILE ACID SEQUESTRANT


    • April 29, 2014
      ✓ 
      Patent use: USE AS A BILE ACID SEQUESTRANT
      ✓ 
      Drug substance


    • April 29, 2014
      ✓ 
      Patent use: USE AS A BILE ACID SEQUESTRANT FOR LOWERING CHOLESTEROL
      ✓ 
      Drug substance


    • October 29, 2014
      ✓ 
      Pediatric exclusivity




  • Amine polymer sequestrant and method of cholesterol depletion
    Patent 5,919,832
    Issued: July 6, 1999
    Inventor(s): Mandeville, III; W. Harry & Holmes-Farley; Stephen Randall
    Assignee(s): Geltex Pharmaceuticals Inc.
    An amine polymer includes first and second substituents bound to amines of the polymer. The first substituent includes a hydrophobic moiety. The second substituent includes a quaternary amine-containing moiety. A method for binding bile salts of bile acids in a mammal includes orally administering to the mammal a therapeutically-effective amount of the amine polymer.
    Patent expiration dates:

    • June 10, 2014


    • April 29, 2014
      ✓ 
      Drug substance


    • December 10, 2014
      ✓ 
      Pediatric exclusivity


    • October 29, 2014
      ✓ 
      Pediatric exclusivity




  • Process for removing bile salts from a patient and alkylated compositions therefor
    Patent 6,066,678
    Issued: May 23, 2000
    Inventor(s): Mandeville, III; W. Harry & Holmes-Farley; Stephen Randall
    Assignee(s): GelTex Pharmaceuticals, Inc.
    The invention relates to a method for removing bile salts from a patient in need thereof and compositions useful in the method. The method comprises administering to the patient a therapeutically effective amount of an alkylated and crosslinked polymer. The alkylated and crosslinked polymer comprises the reaction product of polymers, or salts and copolymers thereof having amine containing repeat units, with at least one aliphatic alkylating agent and a crosslinking agent.
    Patent expiration dates:

    • June 10, 2014
      ✓ 
      Patent use: USE AS A BILE ACID SEQUESTRANT


    • April 29, 2014
      ✓ 
      Patent use: USE AS A BILE ACID SEQUESTRANT
      ✓ 
      Drug substance


    • April 29, 2014
      ✓ 
      Patent use: USE AS A BILE ACID SEQUESTRANT FOR LOWERING CHOLESTEROL
      ✓ 
      Drug substance


    • December 10, 2014
      ✓ 
      Pediatric exclusivity


    • October 29, 2014
      ✓ 
      Pediatric exclusivity




  • Process for removing bile salts from a patient and alkylated compositions therefor
    Patent 6,433,026
    Issued: August 13, 2002
    Inventor(s): W. Harry; Mandeville, III & Stephen Randall; Holmes-Farley
    Assignee(s): GelTex Pharmaceuticals, Inc.
    The invention relates to a method for removing bile salts from a patient in need thereof and compositions useful in the method. The method comprises administering to the patient a therapeutically effective amount of a salt of an alkylated and crosslinked polymer. The alkylated and crosslinked polymer salt comprises the reaction product of crosslinked polymers, or salts and copolymers thereof having amine containing repeat units, with at least one aliphatic alkylating agent.
    Patent expiration dates:

    • June 10, 2014


    • April 29, 2014
      ✓ 
      Drug substance


    • December 10, 2014
      ✓ 
      Pediatric exclusivity


    • October 29, 2014
      ✓ 
      Pediatric exclusivity




  • Process for removing bile salts from a patient and alkylated compositions therefor
    Patent 6,784,254
    Issued: August 31, 2004
    Inventor(s): W. Harry; Mandeville, III & Stephen Randall; Holmes-Farley
    Assignee(s): Genzyme Corporation
    The invention relates to a method for removing bile salts from a patient in need thereof and compositions useful in the method. The method comprises administering to the patient a therapeutically effective amount of a salt of an alkylated and crosslinked polymer. The alkylated and crosslinked polymer salt comprises the reaction product of crosslinked polymers, or salts and copolymers thereof having amine containing repeat units, with at least one aliphatic alkylating agent.
    Patent expiration dates:

    • April 29, 2014
      ✓ 
      Drug substance
      ✓ 
      Drug product


    • October 29, 2014
      ✓ 
      Pediatric exclusivity




  • Process for removing bile salts from a patient and alkylated compositions therefor
    Patent 7,101,960
    Issued: September 5, 2006
    Inventor(s): Mandeville, III; W. Harry & Holmes-Farley; Stephen Randall
    Assignee(s): Genzyme Corporation
    The invention relates to a method for reducing serum cholesterol in a patient in need thereof and alkylated and crosslinked poly(allylamine) polymers useful in the method. The alkylated and crosslinked poly(allylamine) polymers are crosslinked with epichlorohydrin and comprise at least some n-decyl substituted nitrogen atoms and at least some hexyltrimethyl ammonium substituted nitrogen atoms.
    Patent expiration dates:

    • April 29, 2014
      ✓ 
      Patent use: USE AS A BILE ACID SEQUESTRANT FOR LOWERING CHOLESTEROL
      ✓ 
      Drug substance
      ✓ 
      Drug product


    • October 29, 2014
      ✓ 
      Pediatric exclusivity




  • Method for lowering serum glucose
    Patent 7,229,613
    Issued: June 12, 2007
    Inventor(s): Burke; Steven K. & Donovan; Joanne M.
    Assignee(s): Genzyme Corporation
    A method for treating hyperglycemia and/or reducing serum glucose levels in a patient that includes administering to the patient a therapeutically effective amount of an amine polymer is disclosed. In one embodiment, the amine polymer is aliphatic. Examples of polymers useful in an embodiment of the invention include sevelamer hydrogen chloride and colesevelam. The invention includes the use of amine polymers such as a cross-linked polymer characterized by a repeat unit having the formula: and salts and copolymers thereof, where n is a positive integer and x is zero or an integer between 1 and about 4. Also described is a use, for the manufacture of a medicament, of a polymer that lowers serum glucose.
    Patent expiration dates:

    • April 17, 2022
      ✓ 
      Patent use: TREATMENT OF TYPE 2 DIABETES MELLITUS


    • April 17, 2022
      ✓ 
      Patent use: TREATMENT OF TYPE 2 DIABETES MELLITUS


    • October 17, 2022
      ✓ 
      Pediatric exclusivity



Related Exclusivities

Exclusivity is exclusive marketing rights granted by the FDA upon approval of a drug and can run concurrently with a patent or not. Exclusivity is a statutory provision and is granted to an NDA applicant if statutory requirements are met.

  • Exclusivity expiration dates:
    • January 18, 2011 - FOR USE AS AN ADJUNCT TO DIET AND EXERCISE TO IMPROVE GLYCEMIC CONTROL IN ADULTS WITH TYPE 2 DIABETES MELLITUS

    • July 18, 2011 - PEDIATRIC EXCLUSIVITY

    • October 2, 2012 - REDUCE LDL-C LEVELS IN BOYS AND POSTMENARCHAL GIRLS, 10 TO 17 YEARS OF AGE, WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA AS MONOTHERAPY OR IN COMBINATION WITH A STATIN AFTER FAILING AN ADEQUATE TRIAL OF DIET THERAPY

    • April 2, 2013 - PEDIATRIC EXCLUSIVITY

See also...

  • Welchol Consumer Information (Wolters Kluwer)
  • Welchol Suspension Consumer Information (Wolters Kluwer)
  • Welchol Consumer Information (Cerner Multum)
  • Welchol Advanced Consumer Information (Micromedex)
  • WelChol AHFS DI Monographs (ASHP)
  • Colesevelam Consumer Information (Wolters Kluwer)
  • Colesevelam Suspension Consumer Information (Wolters Kluwer)
  • Colesevelam Consumer Information (Cerner Multum)
  • Colesevelam Advanced Consumer Information (Micromedex)
  • Colesevelam Hydrochloride AHFS DI Monographs (ASHP)