FDA NDC Directory · JSON-LD · Markdown

Propranolol Hydrochloride

NDC 60687-215 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA078703
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsPROPRANOLOL HYDROCHLORIDE (60 mg/1)
Marketing started20170301
Package count1

External sources

Source: openFDA. Public-domain (CC0).