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Losartan Potassium and Hydrochlorothiazide

NDC 63187-918 · Proficient Rx LP

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

63187-918-30 — 30 TABLET, FILM COATED in 1 BOTTLE (63187-918-30)

63187-918-60 — 60 TABLET, FILM COATED in 1 BOTTLE (63187-918-60)

63187-918-90 — 90 TABLET, FILM COATED in 1 BOTTLE (63187-918-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63187-571 — Valsartan and Hydrochlorothiazide, 63187-599 — Losartan Potassium and Hydrochlorothiazide, 63187-602 — Losartan Potassium and Hydrochlorothiazide, 63187-653 — Irbesartan and Hydrochlorothiazide, 63187-694 — Valsartan and Hydrochlorothiazide, 63187-708 — Losartan Potassium, 63187-727 — Losartan Potassium and Hydrochlorothiazide, 63187-808 — losartan potassium, 63187-830 — Losartan potassium, 63187-905 — Triamterene and Hydrochlorothiazide, 63187-943 — Valsartan and Hydrochlorothiazide, 63187-981 — Irbesartan and Hydrochlorothiazide, 63629-1068 — Spironolactone and Hydrochlorothiazide, 63629-1069 — Spironolactone and Hydrochlorothiazide, 63629-1071 — Spironolactone and Hydrochlorothiazide, 63629-1218 — Hydrochlorothiazide, 63629-1220 — Hydrochlorothiazide, 63629-2238 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 63629-2239 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 63629-2240 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, +1060 more

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