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olmesartan medoxomil

NDC 71335-0817 · Bryant Ranch Prepack

Generic nameolmesartan medoxomil
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)OLMESARTAN MEDOXOMIL
Strength40 mg/1
Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
Marketing categoryANDA

Packages

71335-0817-1 — 30 TABLET, FILM COATED in 1 BOTTLE (71335-0817-1)

71335-0817-2 — 90 TABLET, FILM COATED in 1 BOTTLE (71335-0817-2)

71335-0817-3 — 28 TABLET, FILM COATED in 1 BOTTLE (71335-0817-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70756-813 — Olmesartan Medoxomil and Hydrochlorothiazide, 70756-814 — Olmesartan Medoxomil and Hydrochlorothiazide, 71205-172 — Olmesartan Medoxomil, 71205-174 — Olmesartan Medoxomil, 71205-458 — Olmesartan Medoxomil, 71205-459 — Olmesartan Medoxomil, 71209-079 — Olmesartan Medoxomil, 71209-080 — Olmesartan Medoxomil, 71209-081 — Olmesartan Medoxomil, 71335-0775 — olmesartan medoxomil, 71335-0845 — Olmesartan Medoxomil and Hydrochlorothiazide, 71335-1920 — olmesartan medoxomil, 71335-2180 — Olmesartan Medoxomil and Hydrochlorothiazide, 71335-2362 — Olmesartan Medoxomil, 71335-2376 — Olmesartan Medoxomil, 71335-2380 — olmesartan medoxomil, 71335-2399 — olmesartan medoxomil, 71335-2424 — olmesartan medoxomil and hydrochlorothiazide, 71335-2425 — olmesartan medoxomil and hydrochlorothiazide, 71335-2448 — 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