FDA NDC Directory · JSON-LD · Markdown

Ezetimibe

NDC 0904-7103 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA209234
Dosage form / routeTABLET · ORAL
Active ingredientsEZETIMIBE (10 mg/1)
Marketing started20171223
Package count2

External sources

Source: openFDA. Public-domain (CC0).