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
- 55111-529_be502229-0e61-8481-dda9-794c93637dd7
- Product NDC
- 55111-529
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- divalproex sodium
- Labeler
- Dr.Reddy's Laboratories Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20080729
- Source listing expiry
- 20261231
Source-listed ingredients
- DIVALPROEX SODIUM — 125 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-529-01) · 55111-529-01
- 500 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-529-05) · 55111-529-05
- 30 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-529-30) · 55111-529-30
- 10 BLISTER PACK in 1 CARTON (55111-529-78) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-529-79) · 55111-529-78
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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