NDC 71335-0008 – Divalproex Sodium
Divalproex Sodium 250 mg/1 · Tablet, Delayed Release · Oral
Product NDC71335-0008
Product details
- Brand name
- Divalproex Sodium
- Generic name
- Divalproex Sodium
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA079163
- Marketed since
- October 1, 2011
- 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 |
|---|---|---|
| 71335-0008-1 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-1) | Dec 21, 2018 |
| 71335-0008-2 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-2) | Mar 6, 2018 |
| 71335-0008-3 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-3) | Mar 1, 2018 |
| 71335-0008-4 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-4) | Dec 27, 2021 |
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