"71335-0783-6" National Drug Code (NDC)

Bupropion Hydrochloride 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0783-6)
(Bryant Ranch Prepack)

NDC Code71335-0783-6
Package Description120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0783-6)
Product NDC71335-0783
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20100409
Marketing Category NameANDA
Application NumberANDA090325
ManufacturerBryant Ranch Prepack
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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