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Mekinist
Mekinist - 0173-0849-13 - (trametinib)
Drug Information of Mekinist
| Product NDC: | 0173-0849 |
| Proprietary Name: | Mekinist |
| Non Proprietary Name: | trametinib |
| Active Ingredient(s): | .5 mg/1 & nbsp; trametinib |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mekinist
| Product NDC: | 0173-0849 |
| Labeler Name: | GlaxoSmithKline LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA204114 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130617 |
Package Information of Mekinist
| Package NDC: | 0173-0849-13 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (0173-0849-13) |
NDC Information of Mekinist
| NDC Code | 0173-0849-13 |
| Proprietary Name | Mekinist |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (0173-0849-13) |
| Product NDC | 0173-0849 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | trametinib |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130617 |
| Marketing Category Name | NDA |
| Labeler Name | GlaxoSmithKline LLC |
| Substance Name | TRAMETINIB DIMETHYL SULFOXIDE |
| Strength Number | .5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
