Divalproex Sodium 68180-0267
Product NDC
68180-0267- Manufacturer
- Lupin Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 29, 2008
- Listing Expires
- December 31, 2027
- Application
- ANDA078790
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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]