NDC 68788-4079 – Divalproex sodium
Divalproex Sodium 250 mg/1 · Tablet, Delayed Release · Oral
Product NDC68788-4079
Product details
- Brand name
- Divalproex sodium
- Generic name
- Divalproex sodium
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078853
- Marketed since
- February 17, 2026
- Listing expires
- December 31, 2027
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 68788-4079-3 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-4079-3) | Feb 17, 2026 |
| 68788-4079-6 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-4079-6) | Feb 17, 2026 |
| 68788-4079-9 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-4079-9) | Feb 17, 2026 |
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