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Diltiazem Hydrochloride Extended-Release

NDC 10370-830 · HUMAN PRESCRIPTION DRUG · CAPSULE, COATED, EXTENDED RELEASE

Generic nameDiltiazem Hydrochloride
Labeler / ManufacturerEndo USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA074984
Dosage form / routeCAPSULE, COATED, EXTENDED RELEASE · ORAL
Active ingredientsDILTIAZEM HYDROCHLORIDE (180 mg/1)
Marketing started20151001
Package count3

External sources

Source: openFDA. Public-domain (CC0).