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"0781-1064-10" National Drug Code (NDC)

Bupropion Hydrochloride 1000 TABLET, FILM COATED in 1 BOTTLE (0781-1064-10)
(Sandoz Inc)

NDC Code0781-1064-10
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (0781-1064-10)
Product NDC0781-1064
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20000207
End Marketing Date20211130
Marketing Category NameANDA
Application NumberANDA075584
ManufacturerSandoz Inc
Substance NameBUPROPION HYDROCHLORIDE
Strength100
Strength Unitmg/1
Pharmacy ClassesAminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0781-1064-10





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