FDA NDC Directory · JSON-LD · Markdown

Benzphetamine Hydrochloride

NDC 23155-952 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202061
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsBENZPHETAMINE HYDROCHLORIDE (50 mg/1)
Marketing started20260619
Package count3

External sources

Source: openFDA. Public-domain (CC0).