United States · FDA National Drug Code directory
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
- 31722-151_4b026ec3-7e85-69ee-e063-6394a90a8c7f
- Product NDC
- 31722-151
- Form
- TABLET, FILM COATED
- Composition / generic term
- Valsartan
- Labeler
- Camber Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210623
- Source listing expiry
- 20271231
Source-listed ingredients
- VALSARTAN — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET, FILM COATED in 1 BOTTLE (31722-151-05) · 31722-151-05
- 30 TABLET, FILM COATED in 1 BOTTLE (31722-151-30) · 31722-151-30
- 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-151-31) · 31722-151-31
- 100 TABLET, FILM COATED in 1 BLISTER PACK (31722-151-32) · 31722-151-32
- 90 TABLET, FILM COATED in 1 BOTTLE (31722-151-90) · 31722-151-90
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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