| NDC Code | 52536-253-03 |
|---|
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (52536-253-03) |
|---|
| Product NDC | 52536-253 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Lamotrigine |
|---|
| Non-Proprietary Name | Lamotrigine |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20140317 |
|---|
| End Marketing Date | 20180531 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA202887 |
|---|
| Manufacturer | Wilshire Pharmaceuticals, Inc. |
|---|
| Substance Name | LAMOTRIGINE |
|---|
| Strength | 200 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
|---|