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
- 42385-931_b47b5c7e-1c20-429c-9560-07f5f06cdce3
- Product NDC
- 42385-931
- Form
- TABLET, FILM COATED
- Composition / generic term
- Sacubitril and Valsartan
- Labeler
- Laurus Labs Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20241111
- 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
- 180 TABLET, FILM COATED in 1 BOTTLE (42385-931-18) · 42385-931-18
- 30 TABLET, FILM COATED in 1 BOTTLE (42385-931-30) · 42385-931-30
- 60 TABLET, FILM COATED in 1 BOTTLE (42385-931-60) · 42385-931-60
- 100 BLISTER PACK in 1 CARTON (42385-931-68) / 10 TABLET, FILM COATED in 1 BLISTER PACK (42385-931-10) · 42385-931-68
- 100 BLISTER PACK in 1 CARTON (42385-931-72) / 10 TABLET, FILM COATED in 1 BLISTER PACK (42385-931-17) · 42385-931-72
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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