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FDA Approved Drugs·

Approval of Wellbutrin, Nda #018644 (Labeling)

Approval Date: 11/05/2025; Drug Name: Wellbutrin, Nda #018644; Active Ingredients: BUPROPION HYDROCHLORIDE; Company: Glaxosmithkline; Submission Status: Approval; Submission Classification: Labeling; Application Number: 018644

Company
GLAXOSMITHKLINE
Keywords
GLAXOSMITHKLINE