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Sacubitril and Valsartan

NDC 70954-975 · ANI Pharmaceuticals, Inc.

Generic nameSacubitril and Valsartan
Dosage formTABLET, FILM COATED
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

70954-975-20 — 60 TABLET, FILM COATED in 1 BOTTLE (70954-975-20)

70954-975-30 — 180 TABLET, FILM COATED in 1 BOTTLE (70954-975-30)

70954-975-50 — 1000 TABLET, FILM COATED in 1 BOTTLE (70954-975-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 70771-1922 — sacubitril and valsartan, 70771-1923 — sacubitril and valsartan, 70954-310 — 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, 71205-327 — Valsartan and Hydrochlorothiazide, 71335-0475 — valsartan, 71335-0547 — Valsartan and Hydrochlorothiazide, +387 more

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

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