Divalproex Sodium 68382-0106
Product NDC
68382-0106- Manufacturer
- Zydus Pharmaceuticals Usa Inc.
- Dosage Form
- Capsule, Coated Pellets
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 27, 2009
- Listing Expires
- December 31, 2027
- Application
- ANDA078919
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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 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-106-01)
1000 CAPSULE, COATED PELLETS in 1 BOTTLE (68382-106-10)
100 BLISTER PACK in 1 CARTON (68382-106-77) / 1 CAPSULE, COATED PELLETS in 1 BLISTER PACK (68382-106-30)