"61919-921-90" National Drug Code (NDC)

Bupropion Hydrochloride 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-921-90)
(DIRECT RX)

NDC Code61919-921-90
Package Description90 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-921-90)
Product NDC61919-921
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20180314
Marketing Category NameANDA
Application NumberANDA075932
ManufacturerDIRECT RX
Substance NameBUPROPION HYDROCHLORIDE
Strength150
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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