Divalproex Sodium 68084-0776
Product NDC
68084-0776- Manufacturer
- American Health Packaging
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 2, 2015
- Listing Expires
- December 31, 2026
- Application
- ANDA090554
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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)
100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-776-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (68084-776-11)