Divalproex Sodium 72162-2316
Product NDC
72162-2316- Manufacturer
- Bryant Ranch Prepack
- 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 | 250 mg/1 |
Drug Class
Anti-epileptic Agent [EPC]Decreased Central Nervous System Disorganized Electrical Activity [PE]Mood Stabilizer [EPC]
Packaging Options(2)
100 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2316-1)
500 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2316-5)