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Propranolol Hydrochloride

NDC 70518-3552 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Generic namepropranolol hydrochloride
Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA212026
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsPROPRANOLOL HYDROCHLORIDE (80 mg/1)
Marketing started20221009
Package count1

External sources

Source: openFDA. Public-domain (CC0).