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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 021515

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WELLBUTRIN XL (BUPROPION HYDROCHLORIDE)
150MG
Marketing Status: Prescription
Active Ingredient: BUPROPION HYDROCHLORIDE
Proprietary Name: WELLBUTRIN XL
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 150MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB3
Application Number: N021515
Product Number: 001
Approval Date: Aug 28, 2003
Applicant Holder Full Name: BAUSCH HEALTH US LLC
Marketing Status:  Prescription
Patent and Exclusivity Information
WELLBUTRIN XL (BUPROPION HYDROCHLORIDE)
300MG
Marketing Status: Prescription
Active Ingredient: BUPROPION HYDROCHLORIDE
Proprietary Name: WELLBUTRIN XL
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 300MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB3
Application Number: N021515
Product Number: 002
Approval Date: Aug 28, 2003
Applicant Holder Full Name: BAUSCH HEALTH US LLC
Marketing Status:  Prescription
Patent and Exclusivity Information
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