Mekinist - 0173-0858-13 - (trametinib)

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Drug Information of Mekinist

Product NDC: 0173-0858
Proprietary Name: Mekinist
Non Proprietary Name: trametinib
Active Ingredient(s): 1    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: 0173-0858
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: 0173-0858-13
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0173-0858-13)

NDC Information of Mekinist

NDC Code 0173-0858-13
Proprietary Name Mekinist
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0173-0858-13)
Product NDC 0173-0858
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 1
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Mekinist


General Information