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Losartan Potassium

NDC 70518-0718 · REMEDYREPACK INC.

Generic nameLosartan Potassium
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)LOSARTAN POTASSIUM
Strength100 mg/1
Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
Marketing categoryANDA

Packages

70518-0718-0 — 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0718-0)

70518-0718-1 — 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0718-1)

70518-0718-3 — 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0718-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68788-8189 — Losartan potassium, 68788-8632 — Losartan Potassium and Hydrochlorothiazide, 68788-8639 — Losartan Potassium, 70010-187 — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE, 70010-188 — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE, 70010-189 — LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE, 70010-741 — Losartan, 70010-742 — Losartan, 70010-743 — Losartan, 70518-0245 — Losartan Potassium, 70518-2132 — Losartan Potassium, 70518-2316 — Losartan Potassium, 70518-2737 — Losartan Potassium and Hydrochlorothiazide, 70518-3282 — Losartan Potassium, 70518-3398 — losartan potassium and hydrochlorothiazide, 70518-3404 — losartan potassium and hydrochlorothiazide, 70518-3420 — losartan potassium and hydrochlorothiazide, 70518-3489 — Losartan Potassium, 70518-3894 — Losartan Potassium, 70518-4289 — Losartan potassium, +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