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Losartan Potassium

NDC 68382-137 · Zydus Pharmaceuticals USA 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

68382-137-01 — 100 TABLET, FILM COATED in 1 BOTTLE (68382-137-01)

68382-137-06 — 30 TABLET, FILM COATED in 1 BOTTLE (68382-137-06)

68382-137-10 — 1000 TABLET, FILM COATED in 1 BOTTLE (68382-137-10)

68382-137-16 — 90 TABLET, FILM COATED in 1 BOTTLE (68382-137-16)

68382-137-77 — 10 BLISTER PACK in 1 CARTON (68382-137-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68382-137-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68180-216 — Losartan Potassium and Hydrochlorothiazide, 68180-217 — Losartan Potassium and Hydrochlorothiazide, 68180-307 — Losartan Potassium, 68180-308 — Losartan Potassium, 68180-309 — Losartan Potassium, 68180-376 — Losartan Potassium, 68180-377 — Losartan Potassium, 68180-378 — Losartan Potassium, 68382-135 — Losartan Potassium, 68382-136 — Losartan Potassium, 68788-4007 — Losartan Potassium, 68788-4091 — Losartan potassium, 68788-4127 — Losartan potassium, 68788-4160 — Losartan, 68788-6452 — Losartan Potassium and Hydrochlorothiazide, 68788-7665 — Losartan Potassium, 68788-8186 — Losartan Potassium, 68788-8187 — losartan potassium and hydrochlorothiazide, 68788-8189 — Losartan potassium, 68788-8632 — Losartan Potassium and Hydrochlorothiazide, +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