FDA NDC Directory · JSON-LD · Markdown

Diltiazem Hydrochloride

NDC 62135-336 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerChartwell RX, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA074093
Dosage form / routeTABLET · ORAL
Active ingredientsDILTIAZEM HYDROCHLORIDE (120 mg/1)
Marketing started19921105
Package count1

External sources

Source: openFDA. Public-domain (CC0).