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LAMOTRIGINE
LAMOTRIGINE - 13668-266-99 - (lamotrigine)
Drug Information of LAMOTRIGINE
| Product NDC: | 13668-266 |
| 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: | 13668-266 |
| Labeler Name: | Torrent Pharmaceuticals Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078947 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090914 |
Package Information of LAMOTRIGINE
| Package NDC: | 13668-266-99 |
| Package Description: | 7 BLISTER PACK in 1 PACKAGE, COMBINATION (13668-266-99) > 1 KIT in 1 BLISTER PACK |
NDC Information of LAMOTRIGINE
| NDC Code | 13668-266-99 |
| Proprietary Name | LAMOTRIGINE |
| Package Description | 7 BLISTER PACK in 1 PACKAGE, COMBINATION (13668-266-99) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 13668-266 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | lamotrigine |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20090914 |
| Marketing Category Name | ANDA |
| Labeler Name | Torrent Pharmaceuticals Limited |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
