| NDC Code: |
0173-0781 |
| Proprietary Name: |
LAMICTAL |
| Suffix: |
XR |
| Non-Proprietary Name: |
lamotrigine |
| Dosage Form: |
TABLET, FILM COATED, EXTENDED RELEASE |
| Method: |
ORAL |
| Original Marketing Date: |
15-08-2011 |
| Category Name: |
NDA |
| Application Number: |
NDA022115 |
| Labeler: |
GLAXOSMITHKLINE LLC |
| Substance Name: |
LAMOTRIGINE |
| Active Numerator Strength: |
250 |
| Active Ingredient Unit: |
mg/1 |
| Pharm Classes: |
Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
| DEA Schedule: |
|
