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Losartan Potassium

NDC 72162-2506 · Bryant Ranch Prepack

Generic nameLosartan Potassium
Dosage formTABLET
RouteORAL
Active ingredient(s)LOSARTAN POTASSIUM
Strength25 mg/1
Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
Marketing categoryANDA

Packages

72162-2506-0 — 1000 TABLET in 1 BOTTLE (72162-2506-0)

72162-2506-3 — 30 TABLET in 1 BOTTLE (72162-2506-3)

72162-2506-9 — 90 TABLET in 1 BOTTLE (72162-2506-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71610-671 — losartan potassium and hydrochlorothiazide, 72162-1696 — losartan potassium, 72162-1697 — losartan potassium, 72162-1698 — losartan potassium, 72162-1700 — losartan potassium and hydrochlorothiazide, 72162-1701 — losartan potassium and hydrochlorothiazide, 72162-2315 — losartan potassium and hydrochlorothiazide, 72162-2461 — losartan potassium and hydrochlorothiazide, 72162-2462 — losartan potassium and hydrochlorothiazide, 72162-2492 — Losartan potassium and Hydrochlorothiazide, 72162-2507 — Losartan Potassium, 72162-2508 — Losartan Potassium, 72189-012 — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE, 72189-082 — LOSARTAN POTASSIUM, 72189-096 — LOSARTAN POTASSIUM, 72189-097 — Losartan Potassium, 72189-098 — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE, 72189-100 — LOSARTAN POTASSIUM, 72189-129 — losartan potassium and hydrochlorothiazide, 72189-139 — losartan potassium and hydrochlorothiazide, +296 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