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
- 27241-115_9d3c5241-441a-491e-9f94-fbca0abcad37
- Product NDC
- 27241-115
- Form
- CAPSULE, COATED PELLETS
- Composition / generic term
- Divalproex sodium
- Labeler
- Ajanta Pharma USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200515
- Source listing expiry
- 20271231
Source-listed ingredients
- DIVALPROEX SODIUM — 125 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE, COATED PELLETS in 1 BOTTLE (27241-115-01) · 27241-115-01
- 500 CAPSULE, COATED PELLETS in 1 BOTTLE (27241-115-05) · 27241-115-05
- 1000 CAPSULE, COATED PELLETS in 1 BOTTLE (27241-115-10) · 27241-115-10
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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