"61786-089-19" National Drug Code (NDC)

Bupropion Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (61786-089-19)
(REMEDYREPACK INC.)

NDC Code61786-089-19
Package Description90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (61786-089-19)
Product NDC61786-089
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20141110
Marketing Category NameANDA
Application NumberANDA076143
ManufacturerREMEDYREPACK 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]

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