NDC 71335-2535 – Divalproex sodium
Divalproex Sodium 500 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC71335-2535
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 · ANDA215527
- Marketed since
- September 26, 2023
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2535-1 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2535-1) | Aug 21, 2026 |
| 71335-2535-2 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2535-2) | Aug 21, 2026 |
| 71335-2535-3 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2535-3) | Nov 22, 2024 |
| 71335-2535-4 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2535-4) | Aug 21, 2026 |
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