Skip to main content

losartan potassium and hydrochlorothiazide

NDC 71335-2662 · Bryant Ranch Prepack

Generic namelosartan potassium and hydrochlorothiazide
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)HYDROCHLOROTHIAZIDE, LOSARTAN POTASSIUM
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

71335-2662-1 — 30 TABLET, FILM COATED in 1 BOTTLE (71335-2662-1)

71335-2662-2 — 90 TABLET, FILM COATED in 1 BOTTLE (71335-2662-2)

71335-2662-3 — 120 TABLET, FILM COATED in 1 BOTTLE (71335-2662-3)

71335-2662-4 — 100 TABLET, FILM COATED in 1 BOTTLE (71335-2662-4)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71335-2425 — olmesartan medoxomil and hydrochlorothiazide, 71335-2558 — Losartan Potassium and Hydrochlorothiazide, 71335-2560 — losartan potassium and hydrochlorothiazide, 71335-2572 — losartan potassium and hydrochlorothiazide, 71335-2589 — Bisoprolol Fumarate and Hydrochlorothiazide, 71335-2616 — Bisoprolol Fumarate and Hydrochlorothiazide, 71335-2617 — valsartan and hydrochlorothiazide, 71335-2618 — valsartan and hydrochlorothiazide, 71335-2631 — Triamterene and Hydrochlorothiazide, 71335-2633 — valsartan and hydrochlorothiazide, 71335-2674 — Spironolactone and Hydrochlorothiazide, 71335-2806 — Triamterene and Hydrochlorothiazide, 71335-2827 — losartan potassium and hydrochlorothiazide, 71335-3029 — OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE, 71335-3030 — OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE, 71335-3031 — OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE, 71335-3048 — Losartan potassium and Hydrochlorothiazide, 71335-3070 — valsartan and hydrochlorothiazide, 71335-9647 — HYDROCHLOROTHIAZIDE, 71335-9686 — olmesartan medoxomil and 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.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels