Losartan Potassium and Hydrochlorothiazide

NDC 65862-469 · Aurobindo Pharma Limited

Generic nameLosartan Potassium and Hydrochlorothiazide

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)LOSARTAN POTASSIUM, HYDROCHLOROTHIAZIDE

Strength12.5; 100 mg/1; mg/1

Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]

Marketing categoryANDA

Packages

65862-469-10 — 10 BLISTER PACK in 1 CARTON (65862-469-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK

65862-469-30 — 30 TABLET, FILM COATED in 1 BOTTLE (65862-469-30)

65862-469-59 — 5000 TABLET, FILM COATED in 1 BOTTLE (65862-469-59)

65862-469-90 — 90 TABLET, FILM COATED in 1 BOTTLE (65862-469-90)

65862-469-99 — 1000 TABLET, FILM COATED in 1 BOTTLE (65862-469-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65862-134 — Hydrochlorothiazide, 65862-161 — QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE, 65862-162 — QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE, 65862-163 — QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE, 65862-201 — Losartan Potassium, 65862-202 — Losartan Potassium, 65862-203 — Losartan Potassium, 65862-308 — Fosinopril Sodium and Hydrochlorothiazide, 65862-309 — Fosinopril Sodium and Hydrochlorothiazide, 65862-468 — Losartan Potassium and Hydrochlorothiazide, 65862-470 — Losartan Potassium and Hydrochlorothiazide, 65862-547 — Valsartan and Hydrochlorothiazide, 65862-548 — Valsartan and Hydrochlorothiazide, 65862-549 — Valsartan and Hydrochlorothiazide, 65862-550 — Valsartan and Hydrochlorothiazide, 65862-551 — Valsartan and Hydrochlorothiazide, 65862-629 — Irbesartan and Hydrochlorothiazide, 65862-630 — Irbesartan and Hydrochlorothiazide, 65862-631 — Irbesartan and Hydrochlorothiazide, 65862-779 — Olmesartan Medoxomil and Hydrochlorothiazide, +1061 more

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