Divalproex Sodium 69452-0434
Product NDC
69452-0434- Manufacturer
- Bionpharma Inc.
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 26, 2024
- Listing Expires
- December 31, 2027
- Application
- ANDA078853
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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(3)
30 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-434-13)
100 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-434-20)
500 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-434-30)