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"59651-532-10" National Drug Code (NDC)

Erlotinib 1 BLISTER PACK in 1 CARTON (59651-532-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK
(Aurobindo Pharma Limited)

NDC Code59651-532-10
Package Description1 BLISTER PACK in 1 CARTON (59651-532-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC59651-532
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameErlotinib
Non-Proprietary NameErlotinib
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20220622
Marketing Category NameANDA
Application NumberANDA216342
ManufacturerAurobindo Pharma Limited
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/59651-532-10





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