Divalproex Sodium 00904-7182-61
- Manufacturer
- Major Pharmaceuticals
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 1, 2015
- Listing Expires
- December 31, 2027
- Application
- ANDA203730
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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]
Selected Package
00904-7182-61Selected100 BLISTER PACK in 1 CARTON (0904-7182-61) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Other packages for this product(1)
80 BLISTER PACK in 1 CARTON (0904-7182-45) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK