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"68382-915-84" National Drug Code (NDC)

Erlotinib 3 BLISTER PACK in 1 CARTON (68382-915-84) / 10 TABLET in 1 BLISTER PACK (68382-915-30)
(Zydus Pharmaceuticals USA Inc.)

NDC Code68382-915-84
Package Description3 BLISTER PACK in 1 CARTON (68382-915-84) / 10 TABLET in 1 BLISTER PACK (68382-915-30)
Product NDC68382-915
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
Strength150
Strength Unitmg/1
Pharmacy ClassesKinase Inhibitor [EPC], Protein Kinase Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68382-915-84





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