Divalproex Sodium 71610-0032
Product NDC
71610-0032- Manufacturer
- Aphena Pharma Solutions - Tennessee, Llc
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 21, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA078182
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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(2)
60 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-032-53)
90 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-032-60)