Divalproex Sodium 68001-0106
Product NDC
68001-0106- Manufacturer
- Bluepoint Laboratories
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 8, 2013
- Listing Expires
- December 31, 2026
- Application
- ANDA078239
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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(2)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-106-00)
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-106-03)