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sacubitril and valsartan

NDC 70710-1272 · Zydus Pharmaceuticals USA Inc.

Generic namesacubitril and valsartan
Dosage formTABLET
RouteORAL
Active ingredient(s)SACUBITRIL, VALSARTAN
Strength24; 26 mg/1; mg/1
Pharmacologic classAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Neprilysin Inhibitor [EPC], Neprilysin Inhibitors [MoA]
Marketing categoryANDA

Packages

70710-1272-4 — 10 BLISTER PACK in 1 CARTON (70710-1272-4) / 10 TABLET in 1 BLISTER PACK (70710-1272-2)

70710-1272-6 — 60 TABLET in 1 BOTTLE (70710-1272-6)

70710-1272-8 — 180 TABLET in 1 BOTTLE (70710-1272-8)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68788-8463 — valsartan and hydrochlorothiazide, 69238-2731 — Sacubitril and Valsartan, 69238-2732 — Sacubitril and Valsartan, 69238-2733 — Sacubitril and Valsartan, 70069-853 — Sacubitril and Valsartan, 70069-854 — Sacubitril and Valsartan, 70069-855 — Sacubitril and Valsartan, 70377-031 — Sacubitril and Valsartan, 70377-032 — Sacubitril and Valsartan, 70377-033 — Sacubitril and Valsartan, 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, +387 more

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