"31722-263-30" National Drug Code (NDC)

Erlotinib 1 BOTTLE in 1 CARTON (31722-263-30) / 30 TABLET, FILM COATED in 1 BOTTLE
(Camber Pharmaceuticals, Inc.)

NDC Code31722-263-30
Package Description1 BOTTLE in 1 CARTON (31722-263-30) / 30 TABLET, FILM COATED in 1 BOTTLE
Product NDC31722-263
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameErlotinib
Non-Proprietary NameErlotinib
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20240524
Marketing Category NameANDA
Application NumberANDA209267
ManufacturerCamber Pharmaceuticals, Inc.
Substance NameERLOTINIB HYDROCHLORIDE
Strength25
Strength Unitmg/1
Pharmacy ClassesKinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA]

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