| NDC Code | 0115-9939-08 |
|---|
| Package Description | 2 BLISTER PACK in 1 CARTON (0115-9939-08) / 15 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0115-9939-68) |
|---|
| Product NDC | 0115-9939 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Lamotrigine |
|---|
| Non-Proprietary Name | Lamotrigine |
|---|
| Dosage Form | TABLET, ORALLY DISINTEGRATING |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20181227 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA200828 |
|---|
| Manufacturer | Amneal Pharmaceuticals of New York LLC |
|---|
| Substance Name | LAMOTRIGINE |
|---|
| Strength | 25 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Dihydrofolate Reductase Inhibitors [MoA], Mood Stabilizer [EPC], Organic Cation Transporter 2 Inhibitors [MoA] |
|---|