Drugplain

Tafinlar 50 mg/1

dabrafenib · CAPSULE · Novartis Pharmaceuticals Corporation

No Recall History
Plain English

Tafinlar (dabrafenib) is an oral prescription capsule used to treat certain types of cancer, particularly melanoma and other cancers with specific genetic mutations. It works by blocking proteins that help cancer cells grow and divide.

Key Facts

Brand Name
Tafinlar
Generic Name
dabrafenib
NDC Code (Product)
0078-0682
Manufacturer
Novartis Pharmaceuticals Corporation
Strength
50 mg/1
Dosage Form
CAPSULE
Route
ORAL
Marketing Status
Application #
NDA202806
Marketing Start
04/12/2016

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

pyrexia4,045 reports
death2,862 reports
malignant neoplasm progression1,737 reports
fatigue1,407 reports
nausea1,382 reports
chills1,314 reports
rash1,156 reports
vomiting971 reports
diarrhoea957 reports
headache737 reports

Frequently Asked Questions

What is Tafinlar used for?

Tafinlar (dabrafenib) is an oral prescription capsule used to treat certain types of cancer, particularly melanoma and other cancers with specific genetic mutations. It works by blocking proteins that help cancer cells grow and divide.

Is Tafinlar a controlled substance?

Tafinlar is not classified as a controlled substance by the DEA.

What is the generic name for Tafinlar?

The generic name for Tafinlar is dabrafenib. There are no other listed brand versions of dabrafenib.

What is the NDC code for Tafinlar 50 mg/1?

The NDC (National Drug Code) for Tafinlar 50 mg/1 is 0078-0682, listed by Novartis Pharmaceuticals Corporation.

Product NDC

0078-0682

Package NDC

0078-0682-66

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)