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
- 48433-034_4c9884d8-fb27-d53c-e063-6294a90a4fe9
- Product NDC
- 48433-034
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- divalproex sodium
- Labeler
- Safecor Health, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260224
- Source listing expiry
- 20271231
Source-listed ingredients
- DIVALPROEX SODIUM — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 80 BLISTER PACK in 1 CARTON (48433-034-08) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (48433-034-01) · 48433-034-08
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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