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U.S. Department of Health and Human Services

Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Search results from the "OB_Rx" table for query on "020358."



Active Ingredient: BUPROPION HYDROCHLORIDE
Dosage Form;Route: TABLET, EXTENDED RELEASE;ORAL
Proprietary Name: WELLBUTRIN SR
Applicant: GLAXOSMITHKLINE
Strength: 100MG
Application Number: N020358
Product Number: 002
Approval Date: Oct 4, 1996
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code: AB1
Patent and Exclusivity Info for this product: View

Active Ingredient: BUPROPION HYDROCHLORIDE
Dosage Form;Route: TABLET, EXTENDED RELEASE;ORAL
Proprietary Name: WELLBUTRIN SR
Applicant: GLAXOSMITHKLINE
Strength: 150MG
Application Number: N020358
Product Number: 003
Approval Date: Oct 4, 1996
Reference Listed Drug No
RX/OTC/DISCN: RX
TE Code: AB1
Patent and Exclusivity Info for this product: View

Active Ingredient: BUPROPION HYDROCHLORIDE
Dosage Form;Route: TABLET, EXTENDED RELEASE;ORAL
Proprietary Name: WELLBUTRIN SR
Applicant: GLAXOSMITHKLINE
Strength: 200MG
Application Number: N020358
Product Number: 004
Approval Date: Jun 14, 2002
Reference Listed Drug Yes
RX/OTC/DISCN: RX
TE Code: AB1
Patent and Exclusivity Info for this product: View

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FDA/Center for Drug Evaluation and Research
Office of Generic Drugs
Division of Labeling and Program Support
Update Frequency:

Orange Book Data - Monthly
Generic Drug Product Information & Patent Information - Daily
Orange Book Data Updated Through October 2014
Patent and Generic Drug Product Data Last Updated November 21, 2014

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