FDA NDC Directory · JSON-LD · Markdown

OLMESARTAN MEDOXOMIL

NDC 72189-137 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / Manufacturerdirect rx
Marketing categoryAbbreviated NDA (generic) · App ANDA207662
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsOLMESARTAN MEDOXOMIL (20 mg/1)
Marketing started20201202
Package count2

External sources

Source: openFDA. Public-domain (CC0).