Divalproex Sodium 51655-0365
Product NDC
51655-0365- Manufacturer
- Northwind Health Company, Llc
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 29, 2020
- 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(1)
30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-365-52)