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"70069-842-01" National Drug Code (NDC)

Tofacitinib 60 TABLET, FILM COATED in 1 BOTTLE (70069-842-01)
(Somerset Therapeutics, LLC)

NDC Code70069-842-01
Package Description60 TABLET, FILM COATED in 1 BOTTLE (70069-842-01)
Product NDC70069-842
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTofacitinib
Non-Proprietary NameTofacitinib
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20260603
Marketing Category NameANDA
Application NumberANDA220137
ManufacturerSomerset Therapeutics, LLC
Substance NameTOFACITINIB CITRATE
Strength10
Strength Unitmg/1
Pharmacy ClassesJanus Kinase Inhibitor [EPC], Janus Kinase Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70069-842-01





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