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"0904-7084-04" National Drug Code (NDC)

Bupropion Hydrochloride 30 BLISTER PACK in 1 CARTON (0904-7084-04) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
(Major Pharmaceuticals)

NDC Code0904-7084-04
Package Description30 BLISTER PACK in 1 CARTON (0904-7084-04) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC0904-7084
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name SuffixXl
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20181201
Marketing Category NameANDA
Application NumberANDA210015
ManufacturerMajor Pharmaceuticals
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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