FDA NDC Directory · JSON-LD · Markdown

Olmesartan Medoxomil

NDC 71205-459 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA206763
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsOLMESARTAN MEDOXOMIL (40 mg/1)
Marketing started20170424
Package count2

External sources

Source: openFDA. Public-domain (CC0).