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sacubitril and valsartan

NDC 70771-1922 · Zydus Lifesciences Limited

Generic namesacubitril and valsartan
Dosage formTABLET
RouteORAL
Active ingredient(s)SACUBITRIL, VALSARTAN
Strength49; 51 mg/1; mg/1
Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Neprilysin Inhibitor [EPC], Neprilysin Inhibitors [MoA]
Marketing categoryANDA

Packages

70771-1922-4 — 10 BLISTER PACK in 1 CARTON (70771-1922-4) / 10 TABLET in 1 BLISTER PACK (70771-1922-2)

70771-1922-6 — 60 TABLET in 1 BOTTLE (70771-1922-6)

70771-1922-8 — 180 TABLET in 1 BOTTLE (70771-1922-8)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 70771-1882 — Valsartan, 70771-1883 — Valsartan, 70771-1884 — Valsartan, 70771-1885 — Valsartan, 70771-1921 — 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, 71205-015 — Valsartan and Hydrochlorothiazide, 71205-042 — Valsartan and Hydrochlorothiazide, 71205-249 — Valsartan and Hydrochlorothiazide, 71205-258 — Valsartan and Hydrochlorothiazide, 71205-301 — 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.