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Valsartan

NDC 70771-1882 · Zydus Lifesciences Limited

Generic nameValsartan
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)VALSARTAN
Strength40 mg/1
Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
Marketing categoryANDA

Packages

70771-1882-3 — 30 TABLET, FILM COATED in 1 BOTTLE (70771-1882-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70710-1273 — sacubitril and valsartan, 70710-1274 — sacubitril and valsartan, 70748-195 — sacubitril and valsartan, 70748-196 — sacubitril and valsartan, 70748-197 — sacubitril and valsartan, 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, 70771-1883 — Valsartan, 70771-1884 — Valsartan, 70771-1885 — Valsartan, 70771-1921 — sacubitril and valsartan, 70771-1922 — sacubitril and valsartan, 70771-1923 — sacubitril and valsartan, 70954-310 — Valsartan, 70954-975 — Sacubitril and Valsartan, 70954-976 — Sacubitril and Valsartan, 70954-977 — Sacubitril and Valsartan, +387 more

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