"0069-0135-01" National Drug Code (NDC)

Bosulif 120 TABLET, FILM COATED in 1 BOTTLE (0069-0135-01)
(Pfizer Laboratories Div Pfizer Inc)

NDC Code0069-0135-01
Package Description120 TABLET, FILM COATED in 1 BOTTLE (0069-0135-01)
Product NDC0069-0135
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBosulif
Non-Proprietary NameBosutinib
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20120904
Marketing Category NameNDA
Application NumberNDA203341
ManufacturerPfizer Laboratories Div Pfizer Inc
Substance NameBOSUTINIB MONOHYDRATE
Strength100
Strength Unitmg/1
Pharmacy ClassesBcr-Abl Tyrosine Kinase Inhibitors [MoA], Kinase Inhibitor [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0069-0135-01