"0069-1001-03" National Drug Code (NDC)

Xeljanz 28 TABLET, FILM COATED in 1 BOTTLE (0069-1001-03)
(Pfizer Laboratories Div Pfizer Inc)

NDC Code0069-1001-03
Package Description28 TABLET, FILM COATED in 1 BOTTLE (0069-1001-03)
Product NDC0069-1001
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameXeljanz
Non-Proprietary NameTofacitinib
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20121109
Marketing Category NameNDA
Application NumberNDA203214
ManufacturerPfizer Laboratories Div Pfizer Inc
Substance NameTOFACITINIB CITRATE
Strength5
Strength Unitmg/1
Pharmacy ClassesJanus Kinase Inhibitor [EPC],Janus Kinase Inhibitors [MoA]

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