"21695-279-90" National Drug Code (NDC)

Bupropion Hydrochloride 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (21695-279-90)
(Rebel Distributors Corp)

NDC Code21695-279-90
Package Description90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (21695-279-90)
Product NDC21695-279
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name SuffixXl
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20081126
Marketing Category NameANDA
Application NumberANDA077715
ManufacturerRebel Distributors Corp
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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