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LAMICTAL
LAMICTAL - 0173-0757-00 - (lamotrigine)
Drug Information of LAMICTAL
| Product NDC: | 0173-0757 |
| Proprietary Name: | LAMICTAL |
| Non Proprietary Name: | lamotrigine |
| Active Ingredient(s): | 200 mg/1 & nbsp; lamotrigine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LAMICTAL
| Product NDC: | 0173-0757 |
| Labeler Name: | GlaxoSmithKline LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022115 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090706 |
Package Information of LAMICTAL
| Package NDC: | 0173-0757-00 |
| Package Description: | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0173-0757-00) |
NDC Information of LAMICTAL
| NDC Code | 0173-0757-00 |
| Proprietary Name | LAMICTAL |
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0173-0757-00) |
| Product NDC | 0173-0757 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | lamotrigine |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20090706 |
| Marketing Category Name | NDA |
| Labeler Name | GlaxoSmithKline LLC |
| Substance Name | LAMOTRIGINE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
