ZELBORAF 240 mg/1
Vemurafenib · TABLET, FILM COATED · Genentech, Inc.
No Recall History
Plain English
ZELBORAF is a tablet, film coated containing vemurafenib at 240 mg/1, taken oral. Manufactured by Genentech, Inc..
Key Facts
- Brand Name
- ZELBORAF
- Generic Name
- Vemurafenib
- NDC Code (Product)
50242-090- Manufacturer
- Genentech, Inc.
- Strength
- 240 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- NDA202429
- Drug Class
- Kinase Inhibitor [EPC]
- Marketing Start
- 08/17/2011
Recall History
No Recall HistoryFrequently Asked Questions
What is ZELBORAF used for?
ZELBORAF contains Vemurafenib. It is a tablet, film coated taken oral. Consult your doctor for specific uses.
Is ZELBORAF a controlled substance?
ZELBORAF is not classified as a controlled substance by the DEA.
What is the generic name for ZELBORAF?
The generic name for ZELBORAF is Vemurafenib. There are no other listed brand versions of Vemurafenib.
What is the NDC code for ZELBORAF 240 mg/1?
The NDC (National Drug Code) for ZELBORAF 240 mg/1 is 50242-090, listed by Genentech, Inc..
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)