"42291-182-50" National Drug Code (NDC)

Bupropion Hydrochloride 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-182-50)
(AvKARE)

NDC Code42291-182-50
Package Description500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-182-50)
Product NDC42291-182
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20221116
End Marketing Date20250331
Marketing Category NameANDA
Application NumberANDA077284
ManufacturerAvKARE
Substance NameBUPROPION HYDROCHLORIDE
Strength150
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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