Divalproex Sodium 55154-2336
Product NDC
55154-2336- Manufacturer
- Cardinal Health 107, Llc
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 29, 2008
- Listing Expires
- December 31, 2026
- Application
- ANDA078597
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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(1)
10 BLISTER PACK in 1 BAG (55154-2336-0) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK