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"68382-914-06" National Drug Code (NDC)

Erlotinib 30 TABLET in 1 BOTTLE (68382-914-06)
(Zydus Pharmaceuticals USA Inc.)

NDC Code68382-914-06
Package Description30 TABLET in 1 BOTTLE (68382-914-06)
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68382-914-06





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