FDA NDC Directory · JSON-LD · Markdown

BUPROPION HYDROCHLORIDE

NDC 72789-301 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA210497
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsBUPROPION HYDROCHLORIDE (150 mg/1)
Marketing started20181108
Package count1

External sources

Source: openFDA. Public-domain (CC0).