FDA NDC Directory · JSON-LD · Markdown

Diltiazem Hydrochloride Extended-Release

NDC 60687-217 · HUMAN PRESCRIPTION DRUG · CAPSULE, COATED, EXTENDED RELEASE

Generic nameDiltiazem Hydrochloride
Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA074984
Dosage form / routeCAPSULE, COATED, EXTENDED RELEASE · ORAL
Active ingredientsDILTIAZEM HYDROCHLORIDE (240 mg/1)
Marketing started20170321
Package count1

External sources

Source: openFDA. Public-domain (CC0).