"68001-199-00" National Drug Code (NDC)

Bupropion Hydrochloride 100 TABLET, FILM COATED in 1 BOTTLE (68001-199-00)
(BluePoint Laboratories)

NDC Code68001-199-00
Package Description100 TABLET, FILM COATED in 1 BOTTLE (68001-199-00)
Product NDC68001-199
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140207
End Marketing Date20190731
Marketing Category NameANDA
Application NumberANDA075584
ManufacturerBluePoint Laboratories
Substance NameBUPROPION HYDROCHLORIDE
Strength75
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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