FDA NDC Directory · JSON-LD · Markdown

Propranolol Hydrochloride

NDC 60687-598 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA070322
Dosage form / routeTABLET · ORAL
Active ingredientsPROPRANOLOL HYDROCHLORIDE (20 mg/1)
Marketing started20211019
Package count1

External sources

Source: openFDA. Public-domain (CC0).