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Propranolol hydrochloride

NDC 70756-296 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerLifestar Pharma LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA216663
Dosage form / routeTABLET · ORAL
Active ingredientsPROPRANOLOL HYDROCHLORIDE (40 mg/1)
Marketing started20260127
Package count2

External sources

Source: openFDA. Public-domain (CC0).