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"0378-7132-93" National Drug Code (NDC)

Erlotinib Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-7132-93)
(Mylan Pharmaceuticals Inc.)

NDC Code0378-7132-93
Package Description30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-7132-93)
Product NDC0378-7132
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameErlotinib Hydrochloride
Non-Proprietary NameErlotinib Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190509
End Marketing Date20221130
Marketing Category NameANDA
Application NumberANDA091002
ManufacturerMylan Pharmaceuticals 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/0378-7132-93





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