| NDC Code: |
68001-106 |
| Proprietary Name: |
Divalproex Sodium |
| Suffix: |
|
| Non-Proprietary Name: |
Divalproex Sodium |
| Dosage Form: |
TABLET, FILM COATED, EXTENDED RELEASE |
| Method: |
ORAL |
| Original Marketing Date: |
08-10-2013 |
| Category Name: |
ANDA |
| Application Number: |
ANDA078239 |
| Labeler: |
BLUEPOINT LABORATORIES |
| Substance Name: |
DIVALPROEX SODIUM |
| Active Numerator Strength: |
500 |
| Active Ingredient Unit: |
mg/1 |
| Pharm Classes: |
Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
| DEA Schedule: |
|
