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
- 60687-915_47e2f52f-946b-05e5-e063-6294a90a5a59
- Product NDC
- 60687-915
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- divalproex sodium
- Labeler
- American Health Packaging
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251229
- Source listing expiry
- 20271231
Source-listed ingredients
- DIVALPROEX SODIUM — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 BLISTER PACK in 1 CARTON (60687-915-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-915-11) · 60687-915-01
- 80 BLISTER PACK in 1 CARTON (60687-915-02) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-915-93) · 60687-915-02
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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