Divalproex Sodium 71335-2124
Product NDC
71335-2124- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 1, 2011
- Listing Expires
- December 31, 2026
- Application
- ANDA079163
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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(4)
60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-1)
30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-2)
90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-3)
100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-4)