"63539-016-02" National Drug Code (NDC)

NDC Code	63539-016-02
Package Description	60 TABLET, FILM COATED in 1 BOTTLE (63539-016-02)
Product NDC	63539-016
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	U.S. Pharmaceuticals
Substance Name	TOFACITINIB CITRATE
Strength	10
Strength Unit	mg/1
Pharmacy Classes	Janus Kinase Inhibitor [EPC], Janus Kinase Inhibitors [MoA]