Skip to main content

OLMESARTAN MEDOXOMIL

NDC 60290-010 · Umedica Laboratories USA Inc.

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

60290-010-01 — 30 TABLET in 1 BOTTLE (60290-010-01)

60290-010-02 — 90 TABLET in 1 BOTTLE (60290-010-02)

60290-010-03 — 10 TABLET in 1 BLISTER PACK (60290-010-03)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51407-198 — olmesartan medoxomil, 51407-199 — olmesartan medoxomil, 51407-857 — amlodipine besylate and olmesartan medoxomil, 51407-858 — amlodipine besylate and olmesartan medoxomil, 51407-859 — amlodipine besylate and olmesartan medoxomil, 51407-860 — amlodipine besylate and olmesartan medoxomil, 59746-463 — olmesartan medoxomil, 59746-465 — olmesartan medoxomil, 59746-466 — olmesartan medoxomil, 60290-009 — OLMESARTAN MEDOXOMIL, 60290-011 — OLMESARTAN MEDOXOMIL, 62135-880 — Olmesartan Medoxomil, 62135-881 — Olmesartan Medoxomil, 62135-882 — Olmesartan Medoxomil, 62332-131 — Olmesartan Medoxomil, 62332-132 — Olmesartan Medoxomil, 62332-133 — Olmesartan Medoxomil, 62332-149 — Olmesartan Medoxomil and Hydrochlorothiazide, 62332-150 — Olmesartan Medoxomil and Hydrochlorothiazide, 62332-151 — Olmesartan Medoxomil and Hydrochlorothiazide, +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