NDC 0078-1105

Mekinist

Trametinib

Mekinist is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Novartis Pharmaceuticals Corporation. The primary component is Trametinib Dimethyl Sulfoxide.

• Product ID: 0078-1105_161c037d-f57b-4ee7-b508-796bde819102
• NDC: 0078-1105
• Product Type: Human Prescription Drug
• Proprietary Name: Mekinist
• Generic Name: Trametinib
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2016-03-17
• Marketing Category: NDA /
• Application Number: NDA204114
• Labeler Name: Novartis Pharmaceuticals Corporation
• Substance Name: TRAMETINIB DIMETHYL SULFOXIDE
• Active Ingredient Strength: 1 mg/1
• Pharm Classes: Kinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 0078-1105-15

30 TABLET, FILM COATED in 1 BOTTLE (0078-1105-15)

• Marketing Start Date: 2021-12-22
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "Mekinist" or generic name "Trametinib"

NDC	Brand Name	Generic Name
0078-0666	Mekinist	trametinib
0078-0668	Mekinist	trametinib
0078-1105	Mekinist	trametinib
0078-1112	Mekinist	trametinib