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Propranolol Hydrochloride

NDC 72789-280 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namepropranolol hydrochloride
Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA070221
Dosage form / routeTABLET · ORAL
Active ingredientsPROPRANOLOL HYDROCHLORIDE (20 mg/1)
Marketing started20100621
Package count1

External sources

Source: openFDA. Public-domain (CC0).