Losartan Potassium
NDC 82009-043 · Quallent Pharmaceuticals Health LLC
Packages
82009-043-10 — 1000 TABLET, FILM COATED in 1 BOTTLE (82009-043-10)
Related Codes
Same active ingredient
FDA lists these products with the same active ingredient.
72789-165 — LOSARTAN POTASSIUM, 72789-179 — LOSARTAN POTASSIUM, 72789-282 — LOSARTAN POTASSIUM, 72865-141 — LOSARTAN POTASSIUM, 72865-142 — LOSARTAN POTASSIUM, 72865-143 — LOSARTAN POTASSIUM, 78206-121 — losartan potassium, 78206-122 — losartan potassium, 78206-123 — losartan potassium, 78206-139 — losartan potassium and hydrochlorothiazide, 78206-140 — losartan potassium and hydrochlorothiazide, 78206-141 — losartan potassium and hydrochlorothiazide, 82009-042 — Losartan Potassium, 82009-044 — Losartan Potassium, 82804-103 — losartan potassium and hydrochlorothiazide, 82804-239 — losartan potassium and hydrochlorothiazide, 83008-086 — losartan potassium and hydrochlorothiazide, 83245-053 — losartan potassium, 87441-052 — Losartan Potassium, 87441-053 — 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