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verapamil hydrochloride

NDC 55289-723 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078906
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsVERAPAMIL HYDROCHLORIDE (240 mg/1)
Marketing started20090917
Package count3

External sources

Source: openFDA. Public-domain (CC0).