"68071-4961-2" National Drug Code (NDC)

Bupropion Hydrochloride 20 TABLET in 1 BOTTLE (68071-4961-2)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-4961-2
Package Description20 TABLET in 1 BOTTLE (68071-4961-2)
Product NDC68071-4961
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20160819
Marketing Category NameANDA
Application NumberANDA206975
ManufacturerNuCare Pharmaceuticals,Inc.
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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