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Propranolol Hydrochloride

NDC 68071-5071 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namepropranolol hydrochloride
Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA070221
Dosage form / routeTABLET · ORAL
Active ingredientsPROPRANOLOL HYDROCHLORIDE (80 mg/1)
Marketing started20100621
Package count1

External sources

Source: openFDA. Public-domain (CC0).