Divalproex Sodium - Divalproex Sodium
Navigation: NDC > Supplier starting with: W > WATSON PHARMA, INC.| Field | Value |
|---|---|
| NDC Code: | 62037-667 |
| Proprietary Name: | Divalproex Sodium |
| Suffix: | |
| Non-Proprietary Name: | Divalproex Sodium |
| Dosage Form: | TABLET, DELAYED RELEASE |
| Method: | ORAL |
| Original Marketing Date: | 25-02-2011 |
| Category Name: | ANDA |
| Application Number: | ANDA079080 |
| Labeler: | WATSON PHARMA, INC. |
| 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: |