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
70377-033_600f67e2-7ccf-65d9-012c-e7ba9b8a089f
Product NDC
70377-033
Form
TABLET, FILM COATED
Composition / generic term
Sacubitril and Valsartan
Labeler
Biocon Pharma Inc.
Marketing category
ANDA
Marketing start / end (source format)
20250717
Source listing expiry
20261231

Source-listed ingredients

  • SACUBITRIL — 97 mg/1
  • VALSARTAN — 103 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, FILM COATED in 1 BOTTLE (70377-033-11) · 70377-033-11
  • 60 TABLET, FILM COATED in 1 BOTTLE (70377-033-12) · 70377-033-12
  • 180 TABLET, FILM COATED in 1 BOTTLE (70377-033-13) · 70377-033-13
  • 500 TABLET, FILM COATED in 1 BOTTLE (70377-033-14) · 70377-033-14

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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