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propranolol hydrochloride

NDC 60760-867 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerST. MARY'S MEDICAL PARK PHARMACY
Marketing categoryAbbreviated NDA (generic) · App ANDA078703
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsPROPRANOLOL HYDROCHLORIDE (60 mg/1)
Marketing started20130311
Package count1

External sources

Source: openFDA. Public-domain (CC0).