NDC 55111-531 – divalproex sodium
Divalproex Sodium 500 mg/1 · Tablet, Delayed Release · Oral
Product NDC55111-531
Product details
- Brand name
- divalproex sodium
- Generic name
- divalproex sodium
- Labeler
- Dr.Reddy's Laboratories Limited
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078755
- Marketed since
- July 29, 2008
- 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 (4)
| Package NDC | Description | Since |
|---|---|---|
| 55111-531-01 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-01) | Jul 29, 2008 |
| 55111-531-05 | 500 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-05) | Jul 29, 2008 |
| 55111-531-30 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-30) | Jul 29, 2008 |
| 55111-531-78 | 10 BLISTER PACK in 1 CARTON (55111-531-78) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-531-79) | Jul 29, 2008 |
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