Divalproex Sodium 68788-8609
Product NDC
68788-8609- Manufacturer
- Preferred Pharmaceuticals Inc.
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 28, 2025
- Listing Expires
- December 31, 2027
- Application
- ANDA078597
Need to source Divalproex Sodium? Find it on a pharmacy-to-pharmacy marketplace at better prices.
✓ DSCSA Compliant. ✓ Verified Pharmacies Only.P2P pharmacy marketplace.
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 (68788-8609-3)
60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8609-6)
90 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8609-9)