FDA NDC Directory · JSON-LD · Markdown

Diltiazem Hydrochloride

NDC 68682-994 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerOCEANSIDE PHARMACEUTICALS
Marketing categoryAbbreviated NDA (generic) · App ANDA075116
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsDILTIAZEM HYDROCHLORIDE (180 mg/1)
Marketing started19991228
Package count1

External sources

Source: openFDA. Public-domain (CC0).