"63539-012-02" National Drug Code (NDC)

Xeljanz 60 TABLET, FILM COATED in 1 BOTTLE (63539-012-02)
(U.S. Pharmaceuticals)

NDC Code63539-012-02
Package Description60 TABLET, FILM COATED in 1 BOTTLE (63539-012-02)
Product NDC63539-012
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameXeljanz
Non-Proprietary NameTofacitinib
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20121108
Marketing Category NameNDA
Application NumberNDA203214
ManufacturerU.S. Pharmaceuticals
Substance NameTOFACITINIB CITRATE
Strength5
Strength Unitmg/1
Pharmacy ClassesJanus Kinase Inhibitor [EPC], Janus Kinase Inhibitors [MoA]

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