"0093-0739-56" National Drug Code (NDC)

Donepezil Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE (0093-0739-56)
(Teva Pharmaceuticals USA Inc)

NDC Code0093-0739-56
Package Description30 TABLET, FILM COATED in 1 BOTTLE (0093-0739-56)
Product NDC0093-0739
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameDonepezil Hydrochloride
Non-Proprietary NameDonepezil Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110531
End Marketing Date20150731
Marketing Category NameANDA
Application NumberANDA090425
ManufacturerTeva Pharmaceuticals USA Inc
Substance NameDONEPEZIL HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesCholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

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