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Diltiazem Hydrochloride

NDC 0641-9219 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078538
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsDILTIAZEM HYDROCHLORIDE (5 mg/mL)
Marketing started20081217
Package count1

External sources

Source: openFDA. Public-domain (CC0).