FDA NDC Directory · JSON-LD · Markdown

Diltiazem Hydrochloride

NDC 50228-482 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerScieGen Pharmaceuticals, Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA216521
Dosage form / routeTABLET · ORAL
Active ingredientsDILTIAZEM HYDROCHLORIDE (60 mg/1)
Marketing started20220926
Package count4

External sources

Source: openFDA. Public-domain (CC0).