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
70954-975_fb8d85f8-7a85-422b-82f0-2a4f5d296b07
Product NDC
70954-975
Form
TABLET, FILM COATED
Composition / generic term
Sacubitril and Valsartan
Labeler
ANI Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20250724
Source listing expiry
20271231

Source-listed ingredients

  • SACUBITRIL — 24 mg/1
  • VALSARTAN — 26 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 60 TABLET, FILM COATED in 1 BOTTLE (70954-975-20) · 70954-975-20
  • 180 TABLET, FILM COATED in 1 BOTTLE (70954-975-30) · 70954-975-30
  • 1000 TABLET, FILM COATED in 1 BOTTLE (70954-975-50) · 70954-975-50

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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