"33261-012-30" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (33261-012-30)
(Aidarex Pharmaceuticals LLC)

NDC Code33261-012-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (33261-012-30)
Product NDC33261-012
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20000207
Marketing Category NameANDA
Application NumberANDA075584
ManufacturerAidarex Pharmaceuticals LLC
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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