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lamotrigine
lamotrigine - 0245-0219-98 - (lamotrigine)
Drug Information of lamotrigine
| Product NDC: | 0245-0219 |
| 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: | 0245-0219 |
| Labeler Name: | Upsher-Smith Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078310 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110228 |
Package Information of lamotrigine
| Package NDC: | 0245-0219-98 |
| Package Description: | 1 BLISTER PACK in 1 PACKAGE, COMBINATION (0245-0219-98) > 1 KIT in 1 BLISTER PACK |
NDC Information of lamotrigine
| NDC Code | 0245-0219-98 |
| Proprietary Name | lamotrigine |
| Package Description | 1 BLISTER PACK in 1 PACKAGE, COMBINATION (0245-0219-98) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 0245-0219 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | lamotrigine |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20110228 |
| Marketing Category Name | ANDA |
| Labeler Name | Upsher-Smith Laboratories, Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
