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"10135-703-30" National Drug Code (NDC)

Bupropion Hydrochloride Extended Release 30 TABLET in 1 BOTTLE (10135-703-30)
(Marlex Pharmaceuticals Inc)

NDC Code10135-703-30
Package Description30 TABLET in 1 BOTTLE (10135-703-30)
Product NDC10135-703
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride Extended Release
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20200701
Marketing Category NameANDA
Application NumberANDA211200
ManufacturerMarlex Pharmaceuticals Inc
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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