NDC Code | 0115-1526-08 |
Package Description | 2 BLISTER PACK in 1 CARTON (0115-1526-08) / 15 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0115-1526-68) |
Product NDC | 0115-1526 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Lamotrigine |
Non-Proprietary Name | Lamotrigine |
Dosage Form | TABLET, ORALLY DISINTEGRATING |
Usage | ORAL |
Start Marketing Date | 20150109 |
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] |