Divalproex Sodium 68001-0473
Product NDC
68001-0473- Manufacturer
- Bluepoint Laboratories
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 20, 2021
- Listing Expires
- December 31, 2027
- Application
- ANDA079163
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Divalproex Sodium | 250 mg/1 |
Drug Class
Anti-epileptic Agent [EPC]Decreased Central Nervous System Disorganized Electrical Activity [PE]Mood Stabilizer [EPC]
Packaging Options(2)
100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-473-00)
500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-473-03)