| NDC Code | 76237-153-30 |
|---|
| Package Description | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-153-30) > 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
|---|
| Product NDC | 76237-153 |
|---|
| 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 | 20120223 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077567 |
|---|
| Manufacturer | McKesson Contract Packaging |
|---|
| Substance Name | DIVALPROEX SODIUM |
|---|
| Strength | 250 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
|---|