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diltiazem hydrochloride

NDC 68382-596 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerZydus Pharmaceuticals (USA) Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA206534
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsDILTIAZEM HYDROCHLORIDE (180 mg/1)
Marketing started20170928
Package count5

External sources

Source: openFDA. Public-domain (CC0).