Divalproex Sodium 68788-8358
Product NDC
68788-8358- Manufacturer
- Preferred Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 13, 2023
- Listing Expires
- December 31, 2027
- Application
- ANDA209286
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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(3)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8358-3)
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8358-6)
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8358-9)