United States · FDA National Drug Code directory

Sacubitril and Valsartan

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
70069-854_0e853a5e-9eab-4bb6-803d-fd9b97e8b550
Product NDC
70069-854
Form
TABLET, FILM COATED
Composition / generic term
Sacubitril and Valsartan
Labeler
Somerset Therapeutics, LLC
Marketing category
ANDA
Marketing start / end (source format)
20260221
Source listing expiry
20271231

Source-listed ingredients

  • SACUBITRIL — 49 mg/1
  • VALSARTAN — 51 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 60 TABLET, FILM COATED in 1 BOTTLE (70069-854-60) · 70069-854-60
  • 180 TABLET, FILM COATED in 1 BOTTLE (70069-854-80) · 70069-854-80

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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Sacubitril and Valsartan — United States | Molindra Medicines