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"72205-082-30" National Drug Code (NDC)

Erlotinib Hydrochloride 1 BOTTLE in 1 CARTON (72205-082-30) > 30 TABLET, FILM COATED in 1 BOTTLE
(Novadoz Pharmaceuticals LLC)

NDC Code72205-082-30
Package Description1 BOTTLE in 1 CARTON (72205-082-30) > 30 TABLET, FILM COATED in 1 BOTTLE
Product NDC72205-082
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameErlotinib Hydrochloride
Non-Proprietary NameErlotinib Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20210511
Marketing Category NameANDA
Application NumberANDA214366
ManufacturerNovadoz Pharmaceuticals LLC
Substance NameERLOTINIB HYDROCHLORIDE
Strength150
Strength Unitmg/1
Pharmacy ClassesKinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/72205-082-30





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