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Losartan Potassium

NDC 71335-0262 · Bryant Ranch Prepack

Generic nameLosartan potassium
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)LOSARTAN POTASSIUM
Strength50 mg/1
Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
Marketing categoryANDA

Packages

71335-0262-1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0262-1)

71335-0262-2 90 TABLET, FILM COATED in 1 BOTTLE (71335-0262-2)

71335-0262-3 60 TABLET, FILM COATED in 1 BOTTLE (71335-0262-3)

71335-0262-4 120 TABLET, FILM COATED in 1 BOTTLE (71335-0262-4)

71335-0262-5 100 TABLET, FILM COATED in 1 BOTTLE (71335-0262-5)

71335-0262-6 180 TABLET, FILM COATED in 1 BOTTLE (71335-0262-6)

71335-0262-7 10 TABLET, FILM COATED in 1 BOTTLE (71335-0262-7)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-3420 — losartan potassium and hydrochlorothiazide, 70518-3489 — Losartan Potassium, 70518-3894 — Losartan Potassium, 70518-4289 — Losartan potassium, 70518-4695 — Losartan Potassium, 71205-226 — Losartan Potassium, 71205-281 — Losartan Potassium, 71205-598 — LOSARTAN POTASSIUM, 71205-675 — LOSARTAN POTASSIUM, 71335-0152 — Losartan Potassium and Hydrochlorothiazide, 71335-1102 — Losartan Potassium, 71335-1136 — losartan potassium, 71335-1174 — Losartan Potassium, 71335-1221 — Losartan Potassium, 71335-1235 — Losartan Potassium, 71335-1580 — Losartan Potassium, 71335-1582 — Losartan Potassium, 71335-1644 — Losartan Potassium, 71335-1817 — losartan potassium, 71335-2083 — Losartan Potassium, +296 more

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