NDC 81469-492 – Divalproex sodium
Divalproex Sodium 125 mg/1 · Capsule, Coated Pellets · Oral
Product NDC81469-492
Product details
- Brand name
- Divalproex sodium
- Generic name
- Divalproex sodium
- Labeler
- First Nation Group, LLC
- Dosage form
- Capsule, Coated Pellets
- Route
- Oral
- Marketing category
- ANDA · ANDA217358
- Marketed since
- November 10, 2025
- Listing expires
- December 31, 2027
- Pharmacologic class
- Anti-epileptic Agent; Mood Stabilizer
Active ingredients
- Divalproex Sodium 125 mg/1
Uses, dosage, side effects and warnings for Divalproex Sodium →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 81469-492-01 | 100 CAPSULE, COATED PELLETS in 1 BOTTLE (81469-492-01) | Nov 10, 2025 |
| 81469-492-10 | 1000 CAPSULE, COATED PELLETS in 1 BOTTLE (81469-492-10) | Nov 10, 2025 |
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