NDC 0069-0136 – Bosulif

Bosutinib Monohydrate 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0069-0136

Product details

Brand name
Bosulif
Generic name
Bosutinib
Labeler
Pfizer Laboratories Div Pfizer Inc
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA203341
Marketed since
September 4, 2012
Listing expires
December 31, 2027
Pharmacologic class
Kinase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Bosulif →

Package NDC codes (1)

Package NDCDescriptionSince
0069-0136-0130 TABLET, FILM COATED in 1 BOTTLE (0069-0136-01)Sep 4, 2012

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