"50090-1768-0" National Drug Code (NDC)

Bupropion Hydrochloride 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-1768-0)
(A-S Medication Solutions)

NDC Code50090-1768-0
Package Description60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-1768-0)
Product NDC50090-1768
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20031125
Marketing Category NameANDA
Application NumberANDA075932
ManufacturerA-S Medication Solutions
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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