Skip to main content

Losartan Potassium and Hydrochlorothiazide

NDC 72789-162 · PD-Rx Pharmaceuticals, Inc.

Generic namelosartan potassium and hydrochlorothiazide
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)LOSARTAN POTASSIUM, HYDROCHLOROTHIAZIDE
Strength12.5; 50 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

72789-162-30 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-162-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72578-114 — bisoprolol fumarate and hydrochlorothiazide, 72578-115 — bisoprolol fumarate and hydrochlorothiazide, 72603-290 — OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE, 72603-291 — OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE, 72603-292 — OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE, 72603-340 — Losartan Potassium, 72603-341 — Losartan Potassium, 72603-342 — Losartan Potassium, 72789-029 — Losartan Potassium, 72789-044 — Losartan Potassium, 72789-163 — LOSARTAN POTASSIUM, 72789-164 — LOSARTAN POTASSIUM, 72789-165 — LOSARTAN POTASSIUM, 72789-176 — Hydrochlorothiazide, 72789-179 — LOSARTAN POTASSIUM, 72789-183 — Triamterene and Hydrochlorothiazide, 72789-282 — LOSARTAN POTASSIUM, 72789-296 — Hydrochlorothiazide, 72789-303 — Hydrochlorothiazide, 72789-381 — 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.