See also: Generic Wellbutrin, Generic Wellbutrin XL
Wellbutrin SR is a brand name of bupropion, approved by the FDA in the following formulation(s):
WELLBUTRIN SR (bupropion hydrochloride - tablet, extended release; oral)
Manufacturer: GLAXOSMITHKLINE
Approval date: October 4, 1996
Strength(s): 100MG [AB1], 150MG [RLD][AB1]
Manufacturer: GLAXOSMITHKLINE
Approval date: June 14, 2002
Strength(s): 200MG [AB1]
Has a generic version of Wellbutrin SR been approved?
A generic version of Wellbutrin SR 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 Wellbutrin SR and have been approved by the FDA:
bupropion hydrochloride tablet, extended release; oral
Manufacturer: ACTAVIS
Approval date: March 12, 2008
Strength(s): 150MG [AB1]
Manufacturer: ACTAVIS
Approval date: July 19, 2010
Strength(s): 100MG [AB1], 200MG [AB1]
Manufacturer: ANCHEN PHARMS
Approval date: June 9, 2011
Strength(s): 100MG [AB1], 150MG [AB1], 200MG [AB1]
Manufacturer: IMPAX LABS
Approval date: January 28, 2004
Strength(s): 100MG [AB1]
Manufacturer: IMPAX LABS
Approval date: March 22, 2004
Strength(s): 150MG [AB1]
Manufacturer: IMPAX LABS
Approval date: December 3, 2004
Strength(s): 200MG [AB1]
Manufacturer: MYLAN
Approval date: April 8, 2010
Strength(s): 100MG [AB1], 150MG [AB1], 200MG [AB1]
Manufacturer: SANDOZ
Approval date: November 25, 2003
Strength(s): 100MG [AB1]
Manufacturer: SANDOZ
Approval date: March 22, 2004
Strength(s): 150MG [AB1]
Manufacturer: SANDOZ
Approval date: June 22, 2005
Strength(s): 200MG [AB1]
Manufacturer: SUN PHARMA GLOBAL
Approval date: April 6, 2010
Strength(s): 100MG [AB1], 150MG [AB1], 200MG [AB1]
Manufacturer: WATSON LABS FLORIDA
Approval date: March 24, 2009
Strength(s): 100MG [AB1], 150MG [AB1], 200MG [AB1]
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Wellbutrin SR. 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 composition containing bupropion hydrochloride and a stabilizer
Patent 5,358,970
Issued: October 25, 1994
Inventor(s): Ruff; Michael D. & Kalidindi; Sanyasi R. & Sutton, Jr.; Joel E.
Assignee(s): Burroughs Wellcome Co.
This application discloses a method of inhibiting degradation of the antidepressant bupropion hydrochloride in a solid pharmaceutical formulation, so that the pharmaceutical formulation will maintain at least 80% of its initial bupropion potency after one year.Patent expiration dates:
- August 12, 2013
- August 12, 2013
Controlled sustained release tablets containing bupropion
Patent 5,427,798
Issued: June 27, 1995
Inventor(s): Ludwig; Jennie Sue G. & Bass, Jr.; William L. & Sutton, Jr.; Joel E.
Assignee(s): Burroughs Wellcome Co.
A controlled sustained release tablet having at least one year shelf life and containing bupropion hydrochloride, hydroxypropyl methylcellulose and cysteine hydrochloride or glycine hydrochloride with the tablet having a surface area to volume ratio to effectively control bupropion hydrochloride release in the body.Patent expiration dates:
- August 12, 2013
- August 12, 2013
Stabilized pharmaceutical composition containing bupropion
Patent 5,731,000
Issued: March 24, 1998
Inventor(s): Ruff; Michael David & Kalidindi; Sanyasi Raju & Sutton, Jr.; Joel Elmore
Assignee(s): Glaxo Wellcome Inc.
This application discloses a method of inhibiting degradation of the antidepressant bupropion hydrochloride in a solid pharmaceutical formulation, so that the pharmaceutical formulation will maintain at least 80% of its initial bupropion potency after one year.Patent expiration dates:
- August 12, 2013
- August 12, 2013
Stabilized pharmaceutical
Patent 5,763,493
Issued: June 9, 1998
Inventor(s): Ruff; Michael D. & Kalidindi; Sanvasi R. & Sutton, Jr.; Joel Elmore
Assignee(s): Glaxo Wellcome Inc.
This application discloses a method of inhibiting degradation of the antidepressant bupropion hydrochloride in a solid pharmaceutical formulation, so that the pharmaceutical formulation will maintain at least 80% of its initial bupropion potency after one year.Patent expiration dates:
- August 12, 2013
- August 12, 2013
See also...
- Wellbutrin SR Sustained-Release Tablets Consumer Information (Wolters Kluwer)
- Wellbutrin SR Consumer Information (Cerner Multum)
- Wellbutrin SR Advanced Consumer Information (Micromedex)
- Bupropion Consumer Information (Drugs.com)
- Bupropion Consumer Information (Wolters Kluwer)
- Bupropion Extended-Release Tablets Consumer Information (Wolters Kluwer)
- Bupropion Hydrobromide Extended-Release Tablets Consumer Information (Wolters Kluwer)
- Bupropion Sustained-Release Tablets Consumer Information (Wolters Kluwer)
- Bupropion Consumer Information (Cerner Multum)
- Bupropion Advanced Consumer Information (Micromedex)
- Bupropion Hydrochloride AHFS DI Monographs (ASHP)
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