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"70771-1521-7" National Drug Code (NDC)

Erlotinib 3 BLISTER PACK in 1 CARTON (70771-1521-7) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1521-2)
(Zydus Lifesciences Limited)

NDC Code70771-1521-7
Package Description3 BLISTER PACK in 1 CARTON (70771-1521-7) / 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1521-2)
Product NDC70771-1521
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameErlotinib
Non-Proprietary NameErlotinib
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200430
Marketing Category NameANDA
Application NumberANDA213065
ManufacturerZydus Lifesciences Limited
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/70771-1521-7





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