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Propranolol Hydrochloride

NDC 71205-590 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA070322
Dosage form / routeTABLET · ORAL
Active ingredientsPROPRANOLOL HYDROCHLORIDE (20 mg/1)
Marketing started20191031
Package count3

External sources

Source: openFDA. Public-domain (CC0).