NDC 63629-4278 – Divalproex Sodium
Divalproex Sodium 500 mg/1 · Tablet, Delayed Release · Oral
Product NDC63629-4278
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 500 mg/1
Uses, dosage, side effects and warnings for Divalproex Sodium →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 63629-4278-1 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-1) | Dec 22, 2021 |
| 63629-4278-2 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-2) | Nov 19, 2012 |
| 63629-4278-3 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-3) | Nov 10, 2014 |
| 63629-4278-4 | 180 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-4) | May 31, 2018 |
| 63629-4278-5 | 120 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-5) | Sep 17, 2018 |
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