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
72603-881_998db1e1-3f32-4812-a64b-5a6870ef7f8f
Product NDC
72603-881
Form
TABLET, FILM COATED
Composition / generic term
Sacubitril and Valsartan
Labeler
NorthStar RxLLC
Marketing category
ANDA
Marketing start / end (source format)
20260629
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 (72603-881-01) · 72603-881-01
  • 180 TABLET, FILM COATED in 1 BOTTLE (72603-881-02) · 72603-881-02

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →