Divalproex Sodium 55111-0532
Product NDC
55111-0532- Manufacturer
- Dr. Reddy's Laboratories Ltd
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 23, 2009
- Listing Expires
- December 31, 2027
- Application
- ANDA078979
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Divalproex Sodium | 125 mg/1 |
Drug Class
Anti-epileptic Agent [EPC]Decreased Central Nervous System Disorganized Electrical Activity [PE]Mood Stabilizer [EPC]
Packaging Options(4)
100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-532-01)
500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-532-05)
30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-532-30)
10 BLISTER PACK in 1 CARTON (55111-532-78) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (55111-532-79)