NDC 55111-532 – Divalproex sodium
Divalproex Sodium 125 mg/1 · Capsule, Delayed Release · Oral
Product NDC55111-532
Product details
- Brand name
- Divalproex sodium
- Generic name
- Divalproex sodium
- Labeler
- Dr. Reddy's Laboratories Ltd
- Dosage form
- Capsule, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078979
- Marketed since
- January 23, 2009
- Listing expires
- December 31, 2027
- Pharmacologic class
- Anti-epileptic Agent; Mood Stabilizer
Active ingredients
- Divalproex Sodium 125 mg/1
Uses, dosage, side effects and warnings for Divalproex Sodium →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 55111-532-01 | 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-532-01) | Jan 23, 2009 |
| 55111-532-05 | 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-532-05) | Jan 23, 2009 |
| 55111-532-30 | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-532-30) | Jan 23, 2009 |
| 55111-532-78 | 10 BLISTER PACK in 1 CARTON (55111-532-78) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (55111-532-79) | Jan 23, 2009 |
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