"16714-334-01" National Drug Code (NDC)

Bupropion Hydrochloride (sr) 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16714-334-01)
(NorthStar RX LLC)

NDC Code16714-334-01
Package Description60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16714-334-01)
Product NDC16714-334
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride (sr)
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20120501
Marketing Category NameANDA
Application NumberANDA077455
ManufacturerNorthStar RX LLC
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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