Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 091459

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BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE)
100MG
Marketing Status: Discontinued

Active Ingredient: BUPROPION HYDROCHLORIDE
Proprietary Name: BUPROPION HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A091459
Product Number: 001
Approval Date: Jun 9, 2011
Applicant Holder Full Name: ANCHEN PHARMACEUTICALS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE)
150MG
Marketing Status: Discontinued

Active Ingredient: BUPROPION HYDROCHLORIDE
Proprietary Name: BUPROPION HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 150MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A091459
Product Number: 002
Approval Date: Jun 9, 2011
Applicant Holder Full Name: ANCHEN PHARMACEUTICALS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE)
200MG
Marketing Status: Discontinued

Active Ingredient: BUPROPION HYDROCHLORIDE
Proprietary Name: BUPROPION HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A091459
Product Number: 003
Approval Date: Jun 9, 2011
Applicant Holder Full Name: ANCHEN PHARMACEUTICALS INC
Marketing Status:  Discontinued
Patent and Exclusivity Information