FDA NDC Directory · JSON-LD · Markdown

Diltiazem Hydrochloride

NDC 16714-555 · HUMAN PRESCRIPTION DRUG · CAPSULE, EXTENDED RELEASE

Labeler / ManufacturerNorthstar Rx LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212317
Dosage form / routeCAPSULE, EXTENDED RELEASE · ORAL
Active ingredientsDILTIAZEM HYDROCHLORIDE (120 mg/1)
Marketing started20220623
Package count1

External sources

Source: openFDA. Public-domain (CC0).