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Sacubitril and Valsartan

NDC 50268-607 · AvPAK

Generic nameSacubitril and Valsartan
Dosage formTABLET, FILM COATED
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

50268-607-15 — 50 BLISTER PACK in 1 BOX (50268-607-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-607-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50228-132 — Valsartan, 50228-133 — Valsartan, 50228-134 — Valsartan, 50228-135 — Valsartan, 50228-147 — valsartan and hydrochlorothiazide, 50228-148 — valsartan and hydrochlorothiazide, 50228-149 — valsartan and hydrochlorothiazide, 50228-150 — valsartan and hydrochlorothiazide, 50228-151 — valsartan and hydrochlorothiazide, 50268-606 — Sacubitril and Valsartan, 50268-608 — Sacubitril and Valsartan, 50268-746 — Valsartan, 50268-747 — Valsartan, 50268-748 — Valsartan, 50268-749 — Valsartan, 51407-668 — amlodipine besylate valsartan hydrochlorothiazide, 51407-669 — amlodipine besylate valsartan hydrochlorothiazide, 51407-670 — amlodipine besylate valsartan hydrochlorothiazide, 51407-671 — amlodipine besylate valsartan hydrochlorothiazide, 51407-672 — amlodipine besylate valsartan 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