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Propranolol Hydrochloride

NDC 51655-302 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namepropranolol hydrochloride
Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA070221
Dosage form / routeTABLET · ORAL
Active ingredientsPROPRANOLOL HYDROCHLORIDE (20 mg/1)
Marketing started20200519
Package count1

External sources

Source: openFDA. Public-domain (CC0).