NDC 67046-1647 – Divalproex sodium
Divalproex Sodium 500 mg/1 · Tablet, Delayed Release · Oral
Product NDC67046-1647
Product details
- Brand name
- Divalproex sodium
- Generic name
- Divalproex sodium
- Labeler
- Coupler LLC
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078853
- Marketed since
- June 26, 2024
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 67046-1647-3 | 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67046-1647-3) | Jun 26, 2024 |
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