Divalproex Sodium 70518-1749
Product NDC
70518-1749- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Capsule, Coated Pellets
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 17, 2018
- Listing Expires
- December 31, 2027
- Application
- ANDA078919
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Divalproex Sodium | 125 mg/1 |
Drug Class
Anti-epileptic Agent [EPC]Decreased Central Nervous System Disorganized Electrical Activity [PE]Mood Stabilizer [EPC]
Packaging Options(1)
100 POUCH in 1 BOX (70518-1749-1) / 1 CAPSULE, COATED PELLETS in 1 POUCH (70518-1749-0)