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"71205-504-30" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-504-30)
(Proficient Rx LP)

NDC Code71205-504-30
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-504-30)
Product NDC71205-504
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20181108
Marketing Category NameANDA
Application NumberANDA210497
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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