FDA NDC Directory · JSON-LD · Markdown

BOSULIF

NDC 0069-0136 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameBosutinib
Labeler / ManufacturerPfizer Laboratories Div Pfizer Inc
Marketing categoryNew Drug Application (innovator) · App NDA203341
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsBOSUTINIB MONOHYDRATE (500 mg/1)
Marketing started20120904
Package count1

External sources

Source: openFDA. Public-domain (CC0).