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
- 68001-646_5872d6ec-adfa-c816-e063-6394a90a9239
- Product NDC
- 68001-646
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- divalproex sodium
- Labeler
- BluePoint Laboratories
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250606
- Source listing expiry
- 20271231
Source-listed ingredients
- DIVALPROEX SODIUM — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-646-00) · 68001-646-00
- 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-646-03) · 68001-646-03
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 →