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"72579-122-01" National Drug Code (NDC)

Brukinsa 1 BOTTLE in 1 CARTON (72579-122-01) / 60 TABLET, FILM COATED in 1 BOTTLE
(BeOne Medicines USA, Inc.)

NDC Code72579-122-01
Package Description1 BOTTLE in 1 CARTON (72579-122-01) / 60 TABLET, FILM COATED in 1 BOTTLE
Product NDC72579-122
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBrukinsa
Non-Proprietary NameZanubrutinib
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20250818
Marketing Category NameNDA
Application NumberNDA218785
ManufacturerBeOne Medicines USA, Inc.
Substance NameZANUBRUTINIB
Strength160
Strength Unitmg/1
Pharmacy ClassesBruton's Tyrosine Kinase Inhibitors [MoA], Kinase Inhibitor [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/72579-122-01





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