| NDC Code | 0228-1435-03 |
|---|
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-1435-03) |
|---|
| Product NDC | 0228-1435 |
|---|
| 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 | 20160401 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA200672 |
|---|
| Manufacturer | Actavis Pharma, Inc. |
|---|
| Substance Name | LAMOTRIGINE |
|---|
| Strength | 50 |
|---|
| 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] |
|---|