NDC 68788-4100 – Divalproex Sodium
Divalproex Sodium 500 mg/1 · Tablet, Extended Release · Oral
Product NDC68788-4100
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA090070
- Marketed since
- April 20, 2026
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 68788-4100-3 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-4100-3) | Apr 20, 2026 |
| 68788-4100-6 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-4100-6) | Apr 20, 2026 |
| 68788-4100-9 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-4100-9) | Apr 20, 2026 |
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