Divalproex Sodium Er 72189-0459
Product NDC
72189-0459- Manufacturer
- Direct_rx
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 3, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA209286
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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)
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-459-60)