NDC 67046-1595 – divalproex sodium
Divalproex Sodium 500 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC67046-1595
Product details
- Brand name
- divalproex sodium
- Generic name
- divalproex sodium
- Labeler
- Coupler LLC
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA214643
- Marketed since
- September 16, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anti-epileptic Agent; Mood Stabilizer
Active ingredients
- Divalproex Sodium 500 mg/1
Uses, dosage, side effects and warnings for Divalproex Sodium →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 67046-1595-3 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (67046-1595-3) | Sep 16, 2025 |
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