DIVALPROEX SODIUM EXTENDED-RELEASE - DIVALPROEX SODIUM EXTENDED-RELEASE
Navigation: NDC > Supplier starting with: A > AMERICAN HEALTH PACKAGING| Field | Value |
|---|---|
| NDC Code: | 68084-316 |
| Proprietary Name: | DIVALPROEX SODIUM EXTENDED-RELEASE |
| Suffix: | |
| Non-Proprietary Name: | DIVALPROEX SODIUM EXTENDED-RELEASE |
| Dosage Form: | TABLET, EXTENDED RELEASE |
| Method: | ORAL |
| Original Marketing Date: | 14-10-2009 |
| Category Name: | ANDA |
| Application Number: | ANDA078705 |
| Labeler: | AMERICAN HEALTH PACKAGING |
| Substance Name: | DIVALPROEX SODIUM |
| Active Numerator Strength: | 250 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
| DEA Schedule: |