United States · FDA National Drug Code directory

Olmesartan Medoxomil

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
72189-373_2c4cb2f6-84b2-31c2-e063-6394a90a5568
Product NDC
72189-373
Form
TABLET, FILM COATED
Composition / generic term
Olmesartan Medoxomil
Labeler
Direct_Rx
Marketing category
ANDA
Marketing start / end (source format)
20220815
Source listing expiry
20261231

Source-listed ingredients

  • OLMESARTAN MEDOXOMIL — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 TABLET, FILM COATED in 1 BOTTLE (72189-373-90) · 72189-373-90

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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