FDA NDC Directory · JSON-LD · Markdown

Ezetimibe

NDC 51660-200 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerOhm Laboratories Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207311
Dosage form / routeTABLET · ORAL
Active ingredientsEZETIMIBE (10 mg/1)
Marketing started20170612
Package count3

External sources

Source: openFDA. Public-domain (CC0).