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"59651-874-01" National Drug Code (NDC)

Bupropion Hydrochloride 100 TABLET, FILM COATED in 1 BOTTLE (59651-874-01)
(Aurobindo Pharma Limited)

NDC Code59651-874-01
Package Description100 TABLET, FILM COATED in 1 BOTTLE (59651-874-01)
Product NDC59651-874
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20240425
Marketing Category NameANDA
Application NumberANDA075491
ManufacturerAurobindo Pharma Limited
Substance NameBUPROPION HYDROCHLORIDE
Strength75
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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