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"50090-2964-0" National Drug Code (NDC)

Bupropion Hydrochloride 32 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-2964-0)
(A-S Medication Solutions)

NDC Code50090-2964-0
Package Description32 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-2964-0)
Product NDC50090-2964
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20031125
Marketing Category NameANDA
Application NumberANDA075932
ManufacturerA-S Medication Solutions
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/50090-2964-0





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