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"0093-7662-56" National Drug Code (NDC)

Erlotinib 30 TABLET, FILM COATED in 1 BOTTLE (0093-7662-56)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-7662-56
Package Description30 TABLET, FILM COATED in 1 BOTTLE (0093-7662-56)
Product NDC0093-7662
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameErlotinib
Non-Proprietary NameErlotinib
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20211208
Marketing Category NameANDA
Application NumberANDA091059
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameERLOTINIB HYDROCHLORIDE
Strength25
Strength Unitmg/1
Pharmacy ClassesKinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-7662-56





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