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Diltiazem Hydrochloride

NDC 0409-4350 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Generic nameDILTIAZEM HYDROCHLORIDE
Labeler / ManufacturerHospira, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075853
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsDILTIAZEM HYDROCHLORIDE (100 mg/1)
Marketing started20050430
Package count1

External sources

Source: openFDA. Public-domain (CC0).