| NDC Code | 0615-7555-05 |
|---|
| Package Description | 15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-7555-05) |
|---|
| Product NDC | 0615-7555 |
|---|
| 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 | 20020228 |
|---|
| End Marketing Date | 20200831 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077567 |
|---|
| Manufacturer | NCS HealthCare of KY, Inc dba Vangard Labs |
|---|
| 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] |
|---|