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Olmesartan Medoxomil

NDC 72189-558 · Direct_rx

Generic nameOlmesartan Medoxomil
Dosage formTABLET
RouteORAL
Active ingredient(s)OLMESARTAN MEDOXOMIL
Strength20 mg/1
Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
Marketing categoryANDA

Packages

72189-558-30 — 30 TABLET in 1 BOTTLE (72189-558-30)

72189-558-90 — 90 TABLET in 1 BOTTLE (72189-558-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-9686 — olmesartan medoxomil and hydrochlorothiazide, 72162-1514 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 72162-1515 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 72162-1516 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 72162-2379 — Amlodipine and Olmesartan Medoxomil, 72189-137 — OLMESARTAN MEDOXOMIL, 72189-138 — OLMESARTAN MEDOXOMIL, 72189-373 — Olmesartan Medoxomil, 72189-548 — Olmesartan Medoxomil, 72189-549 — Olmesartan Medoxomil, 72189-660 — Olmesartan Medoxomil, 72205-147 — olmesartan medoxomil-hydrochlorothiazide, 72205-148 — olmesartan medoxomil-hydrochlorothiazide, 72205-149 — olmesartan medoxomil-hydrochlorothiazide, 72205-165 — Olmesartan medoxomil, 72205-166 — Olmesartan medoxomil, 72205-167 — Olmesartan medoxomil, 72241-078 — Olmesartan Medoxomil, 72241-079 — Olmesartan Medoxomil, 72241-080 — Olmesartan Medoxomil, +281 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels