Drugplain

BOSULIF 400 mg/1

Bosutinib · TABLET, FILM COATED · U.S. Pharmaceuticals

No Recall History
Plain English

BOSULIF is a tablet, film coated containing bosutinib at 400 mg/1, taken oral. Manufactured by U.S. Pharmaceuticals.

Key Facts

Brand Name
BOSULIF
Generic Name
Bosutinib
NDC Code (Product)
63539-193
Manufacturer
U.S. Pharmaceuticals
Strength
400 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
NDA203341
Marketing Start
09/04/2012

Recall History

No Recall History

Frequently Asked Questions

What is BOSULIF used for?

BOSULIF contains Bosutinib. It is a tablet, film coated taken oral. Consult your doctor for specific uses.

Is BOSULIF a controlled substance?

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

What is the generic name for BOSULIF?

The generic name for BOSULIF is Bosutinib. There are 4 other brand versions of Bosutinib.

What is the NDC code for BOSULIF 400 mg/1?

The NDC (National Drug Code) for BOSULIF 400 mg/1 is 63539-193, listed by U.S. Pharmaceuticals.

Product NDC

63539-193

Package NDC

63539-193-30

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

Data from openFDA · Public domain (CC0 1.0)