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"0069-0136-01" National Drug Code (NDC)
Bosulif 30 TABLET, FILM COATED in 1 BOTTLE (0069-0136-01)
(Pfizer Laboratories Div Pfizer Inc)
NDC Code
0069-0136-01
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (0069-0136-01)
Product NDC
0069-0136
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bosulif
Non-Proprietary Name
Bosutinib
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20120904
Marketing Category Name
NDA
Application Number
NDA203341
Manufacturer
Pfizer Laboratories Div Pfizer Inc
Substance Name
BOSUTINIB MONOHYDRATE
Strength
500
Strength Unit
mg/1
Pharmacy Classes
Bcr-Abl Tyrosine Kinase Inhibitors [MoA], Kinase Inhibitor [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0069-0136-01