NDC 71335-2277 – Divalproex Sodium
Divalproex Sodium 250 mg/1 · Tablet, Delayed Release · Oral
Product NDC71335-2277
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078597
- Marketed since
- July 29, 2008
- Listing expires
- December 31, 2026
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2277-1 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2277-1) | Nov 29, 2023 |
| 71335-2277-2 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2277-2) | May 30, 2024 |
| 71335-2277-3 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2277-3) | May 30, 2024 |
| 71335-2277-4 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2277-4) | May 30, 2024 |
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