"33342-528-11" National Drug Code (NDC)

Bupropion Hydrochloride 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-528-11)
(Macleods Pharmaceuticals Limited)

NDC Code33342-528-11
Package Description100 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-528-11)
Product NDC33342-528
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name Suffix(sr)
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20260623
Marketing Category NameANDA
Application NumberANDA218567
ManufacturerMacleods Pharmaceuticals Limited
Substance NameBUPROPION HYDROCHLORIDE
Strength200
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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