FDA NDC Directory · JSON-LD · Markdown

Cardizem LA

NDC 0187-2047 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic nameDiltiazem Hydrochloride
Labeler / ManufacturerBausch Health US LLC
Marketing categoryNew Drug Application (innovator) · App NDA021392
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsDILTIAZEM HYDROCHLORIDE (240 mg/1)
Marketing started20101225
Package count2

External sources

Source: openFDA. Public-domain (CC0).