FDA NDC Directory · JSON-LD · Markdown

OLMESARTAN MEDOXOMIL

NDC 42571-201 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameolmesartan medoxomil
Labeler / ManufacturerMicro Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA206372
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsOLMESARTAN MEDOXOMIL (5 mg/1)
Marketing started20200203
Package count5

External sources

Source: openFDA. Public-domain (CC0).