FDA NDC Directory · JSON-LD · Markdown

DILTIAZEM HCI

NDC 51662-1335 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerHF Acquisition Co LLC, DBA HealthFirst
Marketing categoryAbbreviated NDA (generic) · App ANDA078538
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsDILTIAZEM HYDROCHLORIDE (5 mg/mL)
Marketing started20181221
Package count2

External sources

Source: openFDA. Public-domain (CC0).