"16590-589-30" National Drug Code (NDC)

Budeprion 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16590-589-30)
(STAT RX USA LLC)

NDC Code16590-589-30
Package Description30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16590-589-30)
Product NDC16590-589
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBudeprion
Proprietary Name SuffixXl
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20061214
Marketing Category NameANDA
Application NumberANDA077284
ManufacturerSTAT RX USA LLC
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/16590-589-30