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Diltiazem Hydrochloride

NDC 68682-993 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Generic nameDiltiazem hydrochloride
Labeler / ManufacturerOCEANSIDE PHARMACEUTICALS
Marketing categoryAbbreviated NDA (generic) · App ANDA075116
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsDILTIAZEM HYDROCHLORIDE (120 mg/1)
Marketing started19991228
Package count1

External sources

Source: openFDA. Public-domain (CC0).