"67046-078-30" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-078-30)
(Contract Pharmacy Services-PA)

NDC Code67046-078-30
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (67046-078-30)
Product NDC67046-078
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20060117
Marketing Category NameANDA
Application NumberANDA076143
ManufacturerContract Pharmacy Services-PA
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]

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