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"42292-052-05" National Drug Code (NDC)

Erlotinib Hydrochloride 20 BLISTER PACK in 1 CARTON (42292-052-05) > 1 TABLET, FILM COATED in 1 BLISTER PACK (42292-052-01)
(Mylan Institutional Inc.)

NDC Code42292-052-05
Package Description20 BLISTER PACK in 1 CARTON (42292-052-05) > 1 TABLET, FILM COATED in 1 BLISTER PACK (42292-052-01)
Product NDC42292-052
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameErlotinib Hydrochloride
Non-Proprietary NameErlotinib Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190528
End Marketing Date20210228
Marketing Category NameANDA
Application NumberANDA091002
ManufacturerMylan Institutional Inc.
Substance NameERLOTINIB
Strength100
Strength Unitmg/1
Pharmacy ClassesKinase Inhibitor [EPC],Protein Kinase Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/42292-052-05





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