FDA NDC Directory · JSON-LD · Markdown

Bupropion hydrochloride

NDC 87441-014 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerUnit Dose Solutions, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA215568
Dosage form / routeTABLET · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (300 mg/1)
Marketing started20260608
Package count1

External sources

Source: openFDA. Public-domain (CC0).