United States · FDA National Drug Code directory
Divalproex Sodium
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
- 67046-1571_38f4e70f-be4f-ae1d-e063-6394a90ae3e9
- Product NDC
- 67046-1571
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Divalproex Sodium
- Labeler
- Coupler LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250702
- Source listing expiry
- 20261231
Source-listed ingredients
- DIVALPROEX SODIUM — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67046-1571-3) · 67046-1571-3
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 →