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LOSARTAN POTASSIUM

NDC 71610-465 · Aphena Pharma Solutions - Tennessee, LLC

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

71610-465-30 — 30 TABLET, FILM COATED in 1 BOTTLE (71610-465-30)

71610-465-60 — 90 TABLET, FILM COATED in 1 BOTTLE (71610-465-60)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-2572 — losartan potassium and hydrochlorothiazide, 71335-2662 — losartan potassium and hydrochlorothiazide, 71335-2827 — losartan potassium and hydrochlorothiazide, 71335-3048 — Losartan potassium and Hydrochlorothiazide, 71610-083 — Losartan Potassium, 71610-155 — Losartan Potassium, 71610-207 — Losartan potassium, 71610-224 — Losartan Potassium, 71610-439 — LOSARTAN POTASSIUM, 71610-440 — LOSARTAN POTASSIUM, 71610-466 — Losartan Potassium, 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, +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