Divalproex Sodium 65862-0594
Product NDC
65862-0594- Manufacturer
- Aurobindo Pharma Limited
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 2, 2014
- Listing Expires
- December 31, 2027
- Application
- ANDA202419
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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(5)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-01)
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-05)
10 BLISTER PACK in 1 CARTON (65862-594-10) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-60)
1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-99)