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"50090-7109-0" National Drug Code (NDC)

Bupropion Hydrochloride 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-7109-0)
(A-S Medication Solutions)

NDC Code50090-7109-0
Package Description90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-7109-0)
Product NDC50090-7109
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name Suffix(xl)
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20180830
Marketing Category NameANDA
Application NumberANDA210081
ManufacturerA-S Medication Solutions
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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