NDC 72162-2516 – Divalproex sodium
Divalproex Sodium 500 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC72162-2516
Product details
- Brand name
- Divalproex sodium
- Generic name
- Divalproex sodium
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA202419
- Marketed since
- June 2, 2014
- Listing expires
- December 31, 2026
- 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 (2)
| Package NDC | Description | Since |
|---|---|---|
| 72162-2516-1 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-2516-1) | Jun 9, 2025 |
| 72162-2516-5 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-2516-5) | Jun 9, 2025 |
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