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Diltiazem Hydrochloride

NDC 47335-671 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090421
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsDILTIAZEM HYDROCHLORIDE (240 mg/1)
Marketing started20101115
Package count5

External sources

Source: openFDA. Public-domain (CC0).