"68001-261-04" National Drug Code (NDC)

Bupropion 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-261-04)
(BluePoint Laboratories)

NDC Code68001-261-04
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-261-04)
Product NDC68001-261
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion
Non-Proprietary NameBupropion
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20150122
Marketing Category NameANDA
Application NumberANDA077285
ManufacturerBluePoint Laboratories
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]

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