| NDC Code | 49884-880-86 |
|---|
| Package Description | 30 TABLET, ORALLY DISINTEGRATING in 1 CARTON (49884-880-86) |
|---|
| Product NDC | 49884-880 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Lamotrigine |
|---|
| Non-Proprietary Name | Lamotrigine |
|---|
| Dosage Form | TABLET, ORALLY DISINTEGRATING |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20130602 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA204158 |
|---|
| Manufacturer | Par Pharmaceutical Companies, Inc. |
|---|
| Substance Name | LAMOTRIGINE |
|---|
| Strength | 25 |
|---|
| Strength Unit | 1/1 |
|---|
| Pharmacy Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
|---|