"53217-252-60" National Drug Code (NDC)

Bupropion Hydrochloride 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (53217-252-60)
(Aidarex Pharmaceuticals LLC)

NDC Code53217-252-60
Package Description60 TABLET, EXTENDED RELEASE in 1 BOTTLE (53217-252-60)
Product NDC53217-252
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20160725
Marketing Category NameANDA
Application NumberANDA206674
ManufacturerAidarex Pharmaceuticals LLC
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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