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Diltiazem Hydrochloride

NDC 67046-1492 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameDiltiazem hydrochloride
Labeler / ManufacturerCoupler LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA216521
Dosage form / routeTABLET · ORAL
Active ingredientsDILTIAZEM HYDROCHLORIDE (30 mg/1)
Marketing started20250129
Package count1

External sources

Source: openFDA. Public-domain (CC0).