FDA NDC Directory · JSON-LD · Markdown

Olmesartan Medoxomil

NDC 72189-548 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerDirect_Rx
Marketing categoryAbbreviated NDA (generic) · App ANDA204798
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsOLMESARTAN MEDOXOMIL (20 mg/1)
Marketing started20240419
Package count1

External sources

Source: openFDA. Public-domain (CC0).