Home
>
National Drug Code (NDC)
>
Lamotrigine
Lamotrigine - 51672-4139-6 - (Lamotrigine)
Drug Information of Lamotrigine
| Product NDC: | 51672-4139 |
| Proprietary Name: | Lamotrigine |
| Non Proprietary Name: | Lamotrigine |
| Active Ingredient(s): | 5 mg/1 & nbsp; Lamotrigine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lamotrigine
| Product NDC: | 51672-4139 |
| Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079204 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090204 |
Package Information of Lamotrigine
| Package NDC: | 51672-4139-6 |
| Package Description: | 30 TABLET, CHEWABLE in 1 BOTTLE (51672-4139-6) |
NDC Information of Lamotrigine
| NDC Code | 51672-4139-6 |
| Proprietary Name | Lamotrigine |
| Package Description | 30 TABLET, CHEWABLE in 1 BOTTLE (51672-4139-6) |
| Product NDC | 51672-4139 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Lamotrigine |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20090204 |
| Marketing Category Name | ANDA |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Substance Name | LAMOTRIGINE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE],Mood Stabilizer [EPC] |
