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diltiazem hydrochloride

NDC 50742-252 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerIngenus Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA208783
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsDILTIAZEM HYDROCHLORIDE (360 mg/1)
Marketing started20190614
Package count4

External sources

Source: openFDA. Public-domain (CC0).