"67046-082-07" National Drug Code (NDC)

Bupropion Hydrochloride 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (67046-082-07)
(Contract Pharmacy Services-PA)

NDC Code67046-082-07
Package Description7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (67046-082-07)
Product NDC67046-082
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20170928
Marketing Category NameANDA
Application NumberANDA077284
ManufacturerContract Pharmacy Services-PA
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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