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Trandolapril and Verapamil Hydrochloride

NDC 68462-329 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA079135
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsTRANDOLAPRIL (4 mg/1)
VERAPAMIL HYDROCHLORIDE (240 mg/1)
Marketing started20150225
Package count2

External sources

Source: openFDA. Public-domain (CC0).