Divalproex Sodium 71335-2158
Product NDC
71335-2158- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 24, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA090554
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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(5)
60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-1)
30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-2)
90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-3)
180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-4)
120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-5)