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triamterene and hydrochlorothiazide

NDC 70771-1361 · Zydus Lifesciences Limited

Generic nametriamterene and hydrochlorothiazide
Dosage formTABLET
RouteORAL
Active ingredient(s)TRIAMTERENE, HYDROCHLOROTHIAZIDE
Strength25; 37.5 mg/1; mg/1
Pharmacologic classDecreased Renal K+ Excretion [PE], Increased Diuresis [PE], Increased Diuresis [PE], Potassium-sparing Diuretic [EPC], Thiazide Diuretic [EPC], Thiazides [CS]
Marketing categoryANDA

Packages

70771-1361-0 — 1000 TABLET in 1 BOTTLE (70771-1361-0)

70771-1361-1 — 100 TABLET in 1 BOTTLE (70771-1361-1)

70771-1361-4 — 10 BLISTER PACK in 1 CARTON (70771-1361-4) / 10 TABLET in 1 BLISTER PACK

70771-1361-5 — 500 TABLET in 1 BOTTLE (70771-1361-5)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4577 — OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE, 70756-315 — telmisartan and hydrochlorothiazide, 70756-316 — telmisartan and hydrochlorothiazide, 70756-317 — telmisartan and hydrochlorothiazide, 70756-812 — Olmesartan Medoxomil and Hydrochlorothiazide, 70756-813 — Olmesartan Medoxomil and Hydrochlorothiazide, 70756-814 — Olmesartan Medoxomil and Hydrochlorothiazide, 70771-1325 — candesartan cilexetil and hydrochlorothiazide, 70771-1326 — candesartan cilexetil and hydrochlorothiazide, 70771-1327 — candesartan cilexetil and hydrochlorothiazide, 70771-1362 — triamterene and hydrochlorothiazide, 70771-1474 — Triamterene and Hydrochlorothiazide, 70771-1485 — valsartan and hydrochlorothiazide, 70771-1486 — valsartan and hydrochlorothiazide, 70771-1487 — valsartan and hydrochlorothiazide, 70771-1488 — valsartan and hydrochlorothiazide, 70771-1489 — valsartan and hydrochlorothiazide, 70771-1760 — bisoprolol fumarate and hydrochlorothiazide, 70771-1761 — bisoprolol fumarate and hydrochlorothiazide, 70771-1762 — bisoprolol fumarate and hydrochlorothiazide, +863 more

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