"0591-3332-19" National Drug Code (NDC)

Bupropion Hydrochloride 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0591-3332-19)
(Actavis Pharma, Inc.)

NDC Code0591-3332-19
Package Description90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0591-3332-19)
Product NDC0591-3332
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name SuffixXl
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20070613
End Marketing Date20150731
Marketing Category NameANDA
Application NumberANDA077715
ManufacturerActavis Pharma, Inc.
Substance NameBUPROPION HYDROCHLORIDE
Strength300
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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