"68001-264-03" National Drug Code (NDC)

Bupropion 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-264-03)
(BluePoint Laboratories)

NDC Code68001-264-03
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-264-03)
Product NDC68001-264
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion
Non-Proprietary NameBupropion
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20141003
Marketing Category NameANDA
Application NumberANDA201567
ManufacturerBluePoint Laboratories
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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