| NDC Code | 65841-638-05 |
|---|
| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65841-638-05) |
|---|
| Product NDC | 65841-638 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Divalproex Sodium |
|---|
| Non-Proprietary Name | Divalproex Sodium |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20130107 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078239 |
|---|
| Manufacturer | Zydus Lifesciences Limited |
|---|
| Substance Name | DIVALPROEX SODIUM |
|---|
| Strength | 500 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC] |
|---|