FDA NDC Directory · JSON-LD · Markdown

Propranolol Hydrochloride

NDC 51655-228 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA071972
Dosage form / routeTABLET · ORAL
Active ingredientsPROPRANOLOL HYDROCHLORIDE (40 mg/1)
Marketing started20220819
Package count3

External sources

Source: openFDA. Public-domain (CC0).