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valsartan and hydrochlorothiazide

NDC 70771-1485 · Zydus Lifesciences Limited

Generic namevalsartan and hydrochlorothiazide
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)VALSARTAN, HYDROCHLOROTHIAZIDE
Strength12.5; 80 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

70771-1485-0 — 1000 TABLET, FILM COATED in 1 BOTTLE (70771-1485-0)

70771-1485-4 — 10 BLISTER PACK in 1 CARTON (70771-1485-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK

70771-1485-9 — 90 TABLET, FILM COATED in 1 BOTTLE (70771-1485-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 70771-1361 — triamterene and hydrochlorothiazide, 70771-1362 — triamterene and hydrochlorothiazide, 70771-1474 — Triamterene 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, 70771-1882 — Valsartan, 70771-1883 — Valsartan, 70771-1884 — Valsartan, +1132 more

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