"0069-0136-01" National Drug Code (NDC)

Bosulif 30 TABLET, FILM COATED in 1 BOTTLE (0069-0136-01)
(Pfizer Laboratories Div Pfizer Inc)

NDC Code0069-0136-01
Package Description30 TABLET, FILM COATED in 1 BOTTLE (0069-0136-01)
Product NDC0069-0136
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
Strength500
Strength Unitmg/1
Pharmacy ClassesBcr-Abl Tyrosine Kinase Inhibitors [MoA], Kinase Inhibitor [EPC]

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