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Losartan Potassium and Hydrochlorothiazide

NDC 46708-449 · Alembic Pharmaceuticals 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

46708-449-10 — 100 BLISTER PACK in 1 CARTON (46708-449-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK

46708-449-30 — 30 TABLET, FILM COATED in 1 BOTTLE (46708-449-30)

46708-449-90 — 90 TABLET, FILM COATED in 1 BOTTLE (46708-449-90)

46708-449-91 — 1000 TABLET, FILM COATED in 1 BOTTLE (46708-449-91)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

46708-210 — Telmisartan and Hydrochlorothiazide, 46708-211 — Telmisartan and Hydrochlorothiazide, 46708-438 — Hydrochlorothiazide, 46708-442 — Irbesartan and Hydrochlorothiazide, 46708-443 — Irbesartan and Hydrochlorothiazide, 46708-444 — Irbesartan and Hydrochlorothiazide, 46708-445 — Losartan Potassium, 46708-446 — Losartan Potassium, 46708-447 — Losartan Potassium, 46708-448 — Losartan Potassium and Hydrochlorothiazide, 46708-450 — Losartan Potassium and Hydrochlorothiazide, 46708-453 — Valsartan and Hydrochlorothiazide, 46708-454 — Valsartan and Hydrochlorothiazide, 46708-455 — Valsartan and Hydrochlorothiazide, 46708-456 — Valsartan and Hydrochlorothiazide, 46708-457 — Valsartan and Hydrochlorothiazide, 48433-090 — spironolactone and hydrochlorothiazide, 49884-786 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 49884-787 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, 49884-788 — olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide, +1060 more