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"71205-967-55" National Drug Code (NDC)

Bupropion Hydrochloride 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-967-55)
(Proficient Rx LP)

NDC Code71205-967-55
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-967-55)
Product NDC71205-967
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
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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