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"58118-1064-0" National Drug Code (NDC)

Bupropion Hydrochloride 1 TABLET, FILM COATED in 1 PACKAGE (58118-1064-0)
(Clinical Solutions Wholesale)

NDC Code58118-1064-0
Package Description1 TABLET, FILM COATED in 1 PACKAGE (58118-1064-0)
Product NDC58118-1064
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20000207
Marketing Category NameANDA
Application NumberANDA075584
ManufacturerClinical Solutions Wholesale
Substance NameBUPROPION HYDROCHLORIDE
Strength100
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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