Divalproex Sodium 46708-0821
Product NDC
46708-0821- Manufacturer
- Alembic Pharmaceuticals Limited
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 23, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA218793
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Divalproex Sodium | 125 mg/1 |
Drug Class
Anti-epileptic Agent [EPC]Decreased Central Nervous System Disorganized Electrical Activity [PE]Mood Stabilizer [EPC]
Packaging Options(3)
100 BLISTER PACK in 1 CARTON (46708-821-10) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-821-31)
1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-821-91)