"64679-102-01" National Drug Code (NDC)

Bupropion Hydrochloride 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-102-01)
(Wockhardt USA LLC.)

NDC Code64679-102-01
Package Description30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64679-102-01)
Product NDC64679-102
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 USA LLC.
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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