"55648-102-02" National Drug Code (NDC)

Bupropion Hydrochloride 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55648-102-02)
(Wockhardt Limited)

NDC Code55648-102-02
Package Description90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55648-102-02)
Product NDC55648-102
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name Suffix(xl)
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20121121
Marketing Category NameANDA
Application NumberANDA202189
ManufacturerWockhardt Limited
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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