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"0069-1002-03" National Drug Code (NDC)
Xeljanz 28 TABLET, FILM COATED in 1 BOTTLE (0069-1002-03)
(Pfizer Laboratories Div Pfizer Inc)
NDC Code
0069-1002-03
Package Description
28 TABLET, FILM COATED in 1 BOTTLE (0069-1002-03)
Product NDC
0069-1002
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Xeljanz
Non-Proprietary Name
Tofacitinib
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20180702
Marketing Category Name
NDA
Application Number
NDA203214
Manufacturer
Pfizer Laboratories Div Pfizer Inc
Substance Name
TOFACITINIB CITRATE
Strength
10
Strength Unit
mg/1
Pharmacy Classes
Janus Kinase Inhibitor [EPC],Janus Kinase Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0069-1002-03