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Lamotrigine
Lamotrigine - 0781-4040-67 - (Lamotrigine)
Drug Information of Lamotrigine
| Product NDC: | 0781-4040 |
| Proprietary Name: | Lamotrigine |
| Non Proprietary Name: | Lamotrigine |
| Active Ingredient(s): | & nbsp; Lamotrigine |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lamotrigine
| Product NDC: | 0781-4040 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078645 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100105 |
Package Information of Lamotrigine
| Package NDC: | 0781-4040-67 |
| Package Description: | 1 BLISTER PACK in 1 PACKAGE, COMBINATION (0781-4040-67) > 1 KIT in 1 BLISTER PACK |
NDC Information of Lamotrigine
| NDC Code | 0781-4040-67 |
| Proprietary Name | Lamotrigine |
| Package Description | 1 BLISTER PACK in 1 PACKAGE, COMBINATION (0781-4040-67) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 0781-4040 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Lamotrigine |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20100105 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
