Divalproex Sodium 29300-0138
Product NDC
29300-0138- Manufacturer
- Unichem Pharmaceuticals (usa), Inc.
- Dosage Form
- Tablet, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 1, 2011
- Listing Expires
- December 31, 2027
- Application
- ANDA079163
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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 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-138-01)
500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-138-05)
1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-138-10)