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"46708-127-71" National Drug Code (NDC)

Bupropion Hydrochloride 500 TABLET, FILM COATED in 1 BOTTLE (46708-127-71)
(Alembic Pharmaceuticals Limited)

NDC Code46708-127-71
Package Description500 TABLET, FILM COATED in 1 BOTTLE (46708-127-71)
Product NDC46708-127
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180618
Marketing Category NameANDA
Application NumberANDA203013
ManufacturerAlembic Pharmaceuticals Limited
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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