NDC Active Ingredient Bosutinib Monohydrate

NDC Proprietary Name Non-Proprietary Name Dosage Form Route Name Company Name Product Type
0069-0135Bosulif Bosutinib MonohydrateTablet, Film CoatedOralPfizer Laboratories Div Pfizer IncHuman Prescription Drug
0069-0136Bosulif Bosutinib MonohydrateTablet, Film CoatedOralPfizer Laboratories Div Pfizer IncHuman Prescription Drug
0069-0193Bosulif Bosutinib MonohydrateTablet, Film CoatedOralPfizer Laboratories Div Pfizer IncHuman Prescription Drug
63539-117Bosulif Bosutinib MonohydrateTablet, Film CoatedOralU.s. PharmaceuticalsHuman Prescription Drug

There are 4 NDC products with the active ingredient BOSUTINIB MONOHYDRATE.