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
46708-557_e4716fc9-5f73-4303-8a4e-e8f9129b6e2d
Product NDC
46708-557
Form
TABLET, FILM COATED
Composition / generic term
sacubitril and valsartan
Labeler
Alembic Pharmaceuticals Limited
Marketing category
ANDA
Marketing start / end (source format)
20241104
Source listing expiry
20261231

Source-listed ingredients

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

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 BLISTER PACK in 1 CARTON (46708-557-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 46708-557-10
  • 180 TABLET, FILM COATED in 1 BOTTLE (46708-557-45) · 46708-557-45
  • 60 TABLET, FILM COATED in 1 BOTTLE (46708-557-60) · 46708-557-60
  • 1000 TABLET, FILM COATED in 1 BOTTLE (46708-557-91) · 46708-557-91

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 →