NDC 0615-8587 – divalproex sodium
Divalproex Sodium 250 mg/1 · Tablet, Delayed Release · Oral
Product NDC0615-8587
Product details
- Brand name
- divalproex sodium
- Generic name
- divalproex sodium
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078853
- Marketed since
- June 26, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anti-epileptic Agent; Mood Stabilizer
Active ingredients
- Divalproex Sodium 250 mg/1
Uses, dosage, side effects and warnings for Divalproex Sodium →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0615-8587-39 | 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8587-39) | Aug 15, 2025 |
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