"68382-914-84" National Drug Code (NDC)

Erlotinib 3 BLISTER PACK in 1 CARTON (68382-914-84) / 10 TABLET in 1 BLISTER PACK (68382-914-30)
(Zydus Pharmaceuticals USA Inc.)

NDC Code68382-914-84
Package Description3 BLISTER PACK in 1 CARTON (68382-914-84) / 10 TABLET in 1 BLISTER PACK (68382-914-30)
Product NDC68382-914
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameErlotinib
Non-Proprietary NameErlotinib
Dosage FormTABLET
UsageORAL
Start Marketing Date20200430
Marketing Category NameANDA
Application NumberANDA213065
ManufacturerZydus Pharmaceuticals USA Inc.
Substance NameERLOTINIB HYDROCHLORIDE
Strength100
Strength Unitmg/1
Pharmacy ClassesKinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA]

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