NDC 48433-033 – Divalproex Sodium
Divalproex Sodium 250 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC48433-033
Product details
- Brand name
- Divalproex Sodium
- Generic name
- divalproex sodium
- Labeler
- Safecor Health, LLC
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA077567
- Marketed since
- February 24, 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 48433-033-08 | 80 BLISTER PACK in 1 CARTON (48433-033-08) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (48433-033-01) | Feb 24, 2026 |
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