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DILTIAZEM HYDROCHLORIDE

NDC 50228-498 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic namediltiazem hydrochloride
Labeler / ManufacturerScieGen Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA216327
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsDILTIAZEM HYDROCHLORIDE (300 mg/1)
Marketing started20230406
Package count2

External sources

Source: openFDA. Public-domain (CC0).