| NDC Code | 69117-0047-2 |
|---|
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69117-0047-2) |
|---|
| Product NDC | 69117-0047 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Lamotrigine |
|---|
| Non-Proprietary Name | Lamotrigine Extended-release |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20211209 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA213949 |
|---|
| Manufacturer | Yiling Pharmaceutical, Inc. |
|---|
| Substance Name | LAMOTRIGINE |
|---|
| Strength | 200 |
|---|
| 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] |
|---|