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"53808-0910-1" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (53808-0910-1)
(State of Florida DOH Central Pharmacy)

NDC Code53808-0910-1
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (53808-0910-1)
Product NDC53808-0910
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20090701
Marketing Category NameANDA
Application NumberANDA075491
ManufacturerState of Florida DOH Central Pharmacy
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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