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"71205-565-60" National Drug Code (NDC)

Bupropion 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-565-60)
(Proficient Rx LP)

NDC Code71205-565-60
Package Description60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-565-60)
Product NDC71205-565
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20141101
Marketing Category NameANDA
Application NumberANDA202304
ManufacturerProficient Rx LP
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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