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BENZPHETAMINE HYDROCHLORIDE

NDC 43063-541 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namebenzphetamine hydrochloride
Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090968
Dosage form / routeTABLET · ORAL
Active ingredientsBENZPHETAMINE HYDROCHLORIDE (50 mg/1)
Marketing started20100721
Package count6

External sources

Source: openFDA. Public-domain (CC0).