Divalproex Sodium 55111-0534
Product NDC
55111-0534- Manufacturer
- Dr. Reddy's Laboratories Ltd
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 11, 2013
- Listing Expires
- December 31, 2026
- Application
- ANDA090070
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Divalproex Sodium | 500 mg/1 |
Drug Class
Anti-epileptic Agent [EPC]Decreased Central Nervous System Disorganized Electrical Activity [PE]Mood Stabilizer [EPC]
Packaging Options(4)
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-534-01)
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-534-05)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-534-30)
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-534-60)