"70771-1522-7" National Drug Code (NDC)

Erlotinib 3 BLISTER PACK in 1 CARTON (70771-1522-7) > 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1522-2)
(Cadila Healthcare Limited)

NDC Code70771-1522-7
Package Description3 BLISTER PACK in 1 CARTON (70771-1522-7) > 10 TABLET, FILM COATED in 1 BLISTER PACK (70771-1522-2)
Product NDC70771-1522
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameErlotinib
Non-Proprietary NameErlotinib
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200430
Marketing Category NameANDA
Application NumberANDA213065
ManufacturerCadila Healthcare Limited
Substance NameERLOTINIB HYDROCHLORIDE
Strength100
Strength Unitmg/1
Pharmacy ClassesKinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA]

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