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"50436-0289-1" National Drug Code (NDC)

Bupropion 57 TABLET, EXTENDED RELEASE in 1 BOTTLE (50436-0289-1)
(Unit Dose Services)

NDC Code50436-0289-1
Package Description57 TABLET, EXTENDED RELEASE in 1 BOTTLE (50436-0289-1)
Product NDC50436-0289
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20141101
Marketing Category NameANDA
Application NumberANDA202304
ManufacturerUnit Dose Services
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/50436-0289-1





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