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Diltiazem hydrochloride

NDC 70771-1929 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA219253
Dosage form / routeTABLET · ORAL
Active ingredientsDILTIAZEM HYDROCHLORIDE (30 mg/1)
Marketing started20260525
Package count2

External sources

Source: openFDA. Public-domain (CC0).