"72485-217-30" National Drug Code (NDC)

Erlotinib 1 BOTTLE in 1 BOX (72485-217-30) > 30 TABLET, FILM COATED in 1 BOTTLE
(Armas Pharmaceuticals Inc.)

NDC Code72485-217-30
Package Description1 BOTTLE in 1 BOX (72485-217-30) > 30 TABLET, FILM COATED in 1 BOTTLE
Product NDC72485-217
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameErlotinib
Non-Proprietary NameErlotinib Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20191106
Marketing Category NameANDA
Application NumberANDA211960
ManufacturerArmas Pharmaceuticals Inc.
Substance NameERLOTINIB HYDROCHLORIDE
Strength25
Strength Unitmg/1
Pharmacy ClassesKinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA]

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