Divalproex Sodium 70518-1138
Product NDC
70518-1138- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 25, 2018
- Listing Expires
- December 31, 2027
- Application
- ANDA090161
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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(1)
30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-1138-0)