"31722-439-30" National Drug Code (NDC)

Brexpiprazole 1 BOTTLE in 1 CARTON (31722-439-30) / 30 TABLET, FILM COATED in 1 BOTTLE
(Camber Pharmaceuticals, Inc.)

NDC Code31722-439-30
Package Description1 BOTTLE in 1 CARTON (31722-439-30) / 30 TABLET, FILM COATED in 1 BOTTLE
Product NDC31722-439
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBrexpiprazole
Non-Proprietary NameBrexpiprazole
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20231120
Marketing Category NameANDA
Application NumberANDA213669
ManufacturerCamber Pharmaceuticals, Inc.
Substance NameBREXPIPRAZOLE
Strength4
Strength Unitmg/1
Pharmacy ClassesAtypical Antipsychotic [EPC]

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