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verapamil hydrochloride

NDC 68788-6328 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090700
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsVERAPAMIL HYDROCHLORIDE (120 mg/1)
Marketing started20161017
Package count2

External sources

Source: openFDA. Public-domain (CC0).