FDA NDC Directory · JSON-LD · Markdown

Diltiazem Hydrochloride

NDC 82868-024 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA216521
Dosage form / routeTABLET · ORAL
Active ingredientsDILTIAZEM HYDROCHLORIDE (60 mg/1)
Marketing started20231103
Package count1

External sources

Source: openFDA. Public-domain (CC0).