"72241-021-11" National Drug Code (NDC)

Bupropion Hydrochloride 1000 TABLET, FILM COATED in 1 BOTTLE (72241-021-11)
(Modavar Pharmaceuticals LLC)

NDC Code72241-021-11
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (72241-021-11)
Product NDC72241-021
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200116
Marketing Category NameANDA
Application NumberANDA208606
ManufacturerModavar 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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