FDA NDC Directory · JSON-LD · Markdown

Propranolol Hydrochloride

NDC 72789-372 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA071972
Dosage form / routeTABLET · ORAL
Active ingredientsPROPRANOLOL HYDROCHLORIDE (40 mg/1)
Marketing started20210603
Package count1

External sources

Source: openFDA. Public-domain (CC0).