Divalproex Sodium 00378-0472
Product NDC
00378-0472- Manufacturer
- Mylan Pharmaceuticals Inc.
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 29, 2009
- Listing Expires
- December 31, 2027
- Application
- ANDA077567
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Divalproex Sodium | 250 mg/1 |
Drug Class
Anti-epileptic Agent [EPC]Decreased Central Nervous System Disorganized Electrical Activity [PE]Mood Stabilizer [EPC]
Packaging Options(2)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-0472-01)
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-0472-05)