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Olmesartan Medoxomil

NDC 82009-075 · QUALLENT PHARMACEUTICALS HEALTH LLC

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

82009-075-90 — 90 TABLET, FILM COATED in 1 BOTTLE (82009-075-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72241-078 — Olmesartan Medoxomil, 72241-079 — Olmesartan Medoxomil, 72241-080 — Olmesartan Medoxomil, 72303-0848 — Olmesartan medoxomil, 72303-0849 — Olmesartan medoxomil, 72303-0850 — Olmesartan medoxomil, 72603-290 — OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE, 72603-291 — OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE, 72603-292 — OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE, 72603-950 — Olmesartan medoxomil, 72603-951 — Olmesartan medoxomil, 72603-952 — Olmesartan medoxomil, 73190-078 — olmesartan medoxomil-hydrochlorothiazide, 73190-079 — olmesartan medoxomil-hydrochlorothiazide, 73190-080 — olmesartan medoxomil-hydrochlorothiazide, 82009-073 — Olmesartan Medoxomil, 82009-074 — Olmesartan Medoxomil, 84677-056 — OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE, 84677-057 — OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE, 84677-058 — 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