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Losartan Potassium

NDC 65862-202 · Aurobindo Pharma Limited

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

65862-202-30 — 30 TABLET, FILM COATED in 1 BOTTLE (65862-202-30)

65862-202-90 — 90 TABLET, FILM COATED in 1 BOTTLE (65862-202-90)

65862-202-99 — 1000 TABLET, FILM COATED in 1 BOTTLE (65862-202-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63629-2430 — losartan potassium and hydrochlorothiazide, 63629-2431 — losartan potassium and hydrochlorothiazide, 63629-9192 — losartan potassium, 64380-933 — LOSARTAN POTASSIUM, 64380-934 — LOSARTAN POTASSIUM, 64380-935 — LOSARTAN POTASSIUM, 65841-729 — Losartan Potassium, 65841-730 — Losartan Potassium, 65841-731 — Losartan Potassium, 65862-201 — Losartan Potassium, 65862-203 — Losartan Potassium, 65862-468 — Losartan Potassium and Hydrochlorothiazide, 65862-469 — Losartan Potassium and Hydrochlorothiazide, 65862-470 — Losartan Potassium and Hydrochlorothiazide, 67046-0702 — Losartan Potassium, 67046-1088 — Losartan Potassium, 67046-1470 — Losartan potassium, 67046-1510 — Losartan potassium, 67046-1511 — losartan potassium, 67046-1618 — Losartan Potassium and Hydrochlorothiazide, +296 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.