Thursday, October 6, 2016

Effexor XR


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


EFFEXOR XR (venlafaxine hydrochloride - capsule, extended release; oral)



  • Manufacturer: WYETH PHARMS INC

    Approval date: October 20, 1997

    Strength(s): EQ 150MG BASE [RLD][AB], EQ 37.5MG BASE [AB], EQ 75MG BASE [AB]

Has a generic version of Effexor XR been approved?


A generic version of Effexor XR 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 Effexor XR and have been approved by the FDA:


venlafaxine hydrochloride capsule, extended release; oral



  • Manufacturer: AUROBINDO PHARMA LTD

    Approval date: April 14, 2011

    Strength(s): EQ 150MG BASE [AB], EQ 37.5MG BASE [AB], EQ 75MG BASE [AB]


  • Manufacturer: DR REDDYS LABS LTD

    Approval date: May 6, 2011

    Strength(s): EQ 150MG BASE [AB], EQ 37.5MG BASE [AB], EQ 75MG BASE [AB]


  • Manufacturer: MYLAN

    Approval date: June 1, 2011

    Strength(s): EQ 150MG BASE [AB], EQ 37.5MG BASE [AB], EQ 75MG BASE [AB]


  • Manufacturer: ORCHID HLTHCARE

    Approval date: July 11, 2011

    Strength(s): EQ 150MG BASE [AB], EQ 37.5MG BASE [AB], EQ 75MG BASE [AB]


  • Manufacturer: TEVA

    Approval date: June 28, 2010

    Strength(s): EQ 150MG BASE [AB], EQ 37.5MG BASE [AB], EQ 75MG BASE [AB]


  • Manufacturer: TORRENT PHARMS LLC

    Approval date: June 1, 2011

    Strength(s): EQ 150MG BASE [AB], EQ 37.5MG BASE [AB], EQ 75MG BASE [AB]


  • Manufacturer: VALEANT INTL

    Approval date: April 15, 2011

    Strength(s): EQ 150MG BASE [AB], EQ 37.5MG BASE [AB], EQ 75MG BASE [AB]


  • Manufacturer: WOCKHARDT

    Approval date: April 14, 2011

    Strength(s): EQ 150MG BASE [AB], EQ 37.5MG BASE [AB], EQ 75MG BASE [AB]


  • Manufacturer: ZYDUS PHARMS USA INC

    Approval date: April 14, 2011

    Strength(s): EQ 150MG BASE [AB], EQ 37.5MG BASE [AB], EQ 75MG BASE [AB]

Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Effexor 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


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.




  • Venlafaxine for the treatment of generalized anxiety disorder
    Patent 5,916,923
    Issued: June 29, 1999
    Inventor(s): Rudolph; Richard L. & Upton; G. Virginia
    Assignee(s): American Home Products Corporation
    This invention provides a method of treating obesity, generalized anxiety disorder, post-traumatic stress disorder, late luteal phase disphoric disorder (premenstrual syndrome), attention deficit disorder, with and without hyperactivity, Gilles de la Tourette syndrome, bulimia iervosa or Shy Drager Syndrome in a mammal by administering to the mammal an effective amount of a hydroxycycloalkanephenethyl amine of the following structural formula: ##STR1## in which A is a moiety of the formula ##STR2## where the dotted line represents optional unsaturation; R.sub.1 is hydrogen or alkyl; R.sub.2 is alkyl; R.sub.4 is hydrogen, alkyl, formyl, or alkanol; R.sub.5 and R.sub.6 are, independently, hydrogen, hydroxyl, aakyl, alkoxy, alkanoyloxy, cyano, nitro, alkylmercapto, amino, alkylamino, dialkylamino, alkanamido, halo, trifluoromethyl, or taken together, methylene dioxy; R.sub.7 is hydrogen or alkyl; and n is 0, 1, 2, 3, or 4; or a pharmaceutically acceptable salt thereof.
    Patent expiration dates:

    • June 28, 2013
      ✓ 
      Patent use: TREATMENT OF GENERALIZED ANXIETY DISORDER


    • December 28, 2013
      ✓ 
      Patent use: TREATMENT OF GENERALIZED ANXIETY DISORDER
      ✓ 
      Pediatric exclusivity




  • Extended release formulation of venlafaxine hydrochloride
    Patent 6,274,171
    Issued: August 14, 2001
    Inventor(s): Sherman; Deborah M. & Clark; John C. & Lamer; John U. & White; Steven A.
    Assignee(s): American Home Products Corporation
    This invention relates to a 24 hour extended release dosage formulation and unit dosage form thereof of venlafaxine hydrochloride, an antidepressant, which provides better control of blood plasma levels than conventional tablet formulations which must be administered two or more times a day and further provides a lower incidence of nausea and vomiting than the conventional tablets. More particularly, the invention comprises an extended release formulation of venlafaxine hydrochloride comprising a therapeutically effective amount of venlafaxine hydrochloride in spheroids comprised of venlafaxine hydrochloride, microcrystalline cellulose and, optionally, hydroxypropylmethylcellulose coated with a mixture of ethyl cellulose and hydroxypropylmethylcellulose.
    Patent expiration dates:

    • March 20, 2017


    • September 20, 2017
      ✓ 
      Pediatric exclusivity




  • Treatments using venlafaxine
    Patent 6,310,101
    Issued: October 30, 2001
    Inventor(s): Rudolph; Richard L. & Derivan; Albert T. & Muth; Eric A. & Upton; G. Virginia
    Assignee(s): American Home Products Corporation
    This invention provides a method of treating obesity, generalized anxiety disorder, post-traumatic stress disorder, late luteal phase disphoric disorder (premenstrual syndrome), attention deficit disorder, with and without hyperactivity, Gilles de la Tourette syndrome, bulimia nervosa or Shy Drager Syndrome in a mammal by administering to the mammal an effective amount of a hydroxycycloalkanephenethyl amine of the following structural formula: ##STR1## in which A is a moiety of the formula ##STR2## where the dotted line represents optional unsaturation; R.sub.1 is hydrogen or alkyl; R.sub.2 is alkyl; R.sub.4 is hydrogen, alkyl, formyl, or alkanol; R.sub.5 and R.sub.6 are, independently, hydrogen, hydroxyl, alkyl, alkoxy, alkanoyloxy, cyano, nitro, alkylmercapto, amino, alkylamino, dialkylamino, alkanamido, halo, trifluoromethyl, or taken together, methylene dioxy; R.sub.7 is hydrogen or alkyl; and n is 0, 1, 2, 3, or 4; or a pharmaceutically acceptable salt thereof.
    Patent expiration dates:

    • June 28, 2013
      ✓ 
      Patent use: TREATMENT OF PANIC DISORDER




  • Extended release formulation of venlafaxine hydrochloride
    Patent 6,403,120
    Issued: June 11, 2002
    Inventor(s): Deborah M.; Sherman & John C.; Clark & John U.; Lamer & Steven A.; White
    Assignee(s): Wyeth
    This invention relates to a 24 hour extended release dosage formulation and unit dosage form thereof of venlafaxine hydrochloride, an antidepressant, which provides better control of blood plasma levels than conventional tablet formulations which must be administered two or more times a day and fiber provides a lower incidence of nausea and vomiting than the conventional tablets. More particularly, the invention comprises an extended release formulation of venlafaxine hydrochloride comprising a therapeutically effective amount of venlafaxine hydrochloride in spheroids comprised of venlafaxine hydrochloride, microcrystalline cellulose and, optionally, hydroxypropylmethylcellulose coated with a mixture of ethyl cellulose and hydroxypropylmethylcellulose.
    Patent expiration dates:

    • March 20, 2017
      ✓ 
      Patent use: TREATMENT OF DEPRESSION AND GENERALIZED ANXIETY DISORDER


    • March 20, 2017
      ✓ 
      Patent use: TREATMENT OF SOCIAL ANXIETY DISORDER


    • September 20, 2017
      ✓ 
      Patent use: TREATMENT OF SOCIAL ANXIETY DISORDER
      ✓ 
      Pediatric exclusivity


    • September 20, 2017
      ✓ 
      Patent use: TREATMENT OF DEPRESSION AND GENERALIZED ANXIETY DISORDER
      ✓ 
      Pediatric exclusivity




  • Extended release formulation of venlafaxine hydrochloride
    Patent 6,419,958
    Issued: July 16, 2002
    Inventor(s): Deborah M.; Sherman & John C.; Clark & John U.; Lamer & Steven A.; White
    Assignee(s): Wyeth
    This invention relates to a 24 hour extended release dosage formulation and unit dosage form thereof of venlafaxine hydrochloride, an antidepressant, which provides better control of blood plasma levels than conventional tablet formulations which must be administered two or more times a day and further provides a lower incidence of nausea and vomiting than the conventional tablets. More particularly, the invention comprises an extended release formulation of venlafaxine hydrochloride comprising a therapeutically effective amount of venlafaxine hydrochloride in spheroids comprised of venlafaxine hydrochloride, microcrystalline cellulose and, optionally, hydroxypropylmethylcellulose coated with a mixture of ethyl cellulose and hydroxypropylmethylcellulose.
    Patent expiration dates:

    • March 20, 2017
      ✓ 
      Patent use: TREATMENT OF SOCIAL ANXIETY DISORDER


    • March 20, 2017
      ✓ 
      Patent use: TREATMENT OF DEPRESSION AND GENERALIZED ANXIETY DISORDER


    • September 20, 2017
      ✓ 
      Patent use: TREATMENT OF DEPRESSION AND GENERALIZED ANXIETY DISORDER
      ✓ 
      Pediatric exclusivity


    • September 20, 2017
      ✓ 
      Patent use: TREATMENT OF SOCIAL ANXIETY DISORDER
      ✓ 
      Pediatric exclusivity




  • Treatment using venlafaxine
    Patent 6,444,708
    Issued: September 3, 2002
    Inventor(s): Richard L.; Rudolph & Albert T.; Derivan & G. Virginia; Upton
    Assignee(s): Wyeth
    This invention provides a method of treating obesity, generalized anxiety disorder, post-traumatic stress disorder, late luteal phase disphoric disorder (premenstrual syndrome), attention deficit disorder, with and without hyperactivity, Gilles de la Tourette syndrome, bulimia nervosa or Shy Drager Syndrome in a mammal by administering to the mammal an effective amount of a hydroxycycloalkanephenethyl amine of the following structural formula: in which A is a moiety of the formula where the dotted line represents optional unsaturation; R1 is hydrogen or alkyl; R2 is alkyl; R4 is hydrogen, alkyl, formyl, or alkanol; R5 and R6 are, independently, hydrogen, hydroxyl, alkyl, alkoxy, alkanoyloxy, cyano, nitro, alkylmercapto, amino, alkylamino, dialkylamino, alkanamido, halo, trifluoromethyl, or taken together, methylene dioxy; R7 is hydrogen or alkyl; and n is 0, 1, 2, 3, or 4; or a pharmaceutically acceptable salt thereof.
    Patent expiration dates:

    • June 28, 2013
      ✓ 
      Patent use: TREATMENT OF GENERALIZED ANXIETY DISORDER


    • December 28, 2013
      ✓ 
      Patent use: TREATMENT OF GENERALIZED ANXIETY DISORDER
      ✓ 
      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:
    • December 14, 2010 - LONG-TERM TREATMENT OF SOCIAL ANXIETY DISORDER

See also...

  • Effexor XR Extended-Release Capsules Consumer Information (Wolters Kluwer)
  • Effexor XR Extended-Release Tablets Consumer Information (Wolters Kluwer)
  • Effexor XR Consumer Information (Cerner Multum)
  • Effexor-XR Advanced Consumer Information (Micromedex)
  • Venlafaxine Consumer Information (Drugs.com)
  • Venlafaxine Consumer Information (Wolters Kluwer)
  • Venlafaxine Extended-Release Capsules Consumer Information (Wolters Kluwer)
  • Venlafaxine Extended-Release Tablets Consumer Information (Wolters Kluwer)
  • Venlafaxine Consumer Information (Cerner Multum)
  • Venlafaxine Advanced Consumer Information (Micromedex)
  • Venlafaxine Hydrochloride AHFS DI Monographs (ASHP)

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