"69367-289-09" National Drug Code (NDC)

Bupropion Hydrochloride 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-289-09)
(Westminster Pharmaceuticals, LLC)

NDC Code69367-289-09
Package Description90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-289-09)
Product NDC69367-289
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Proprietary Name SuffixXl
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20171001
Marketing Category NameANDA
Application NumberANDA207224
ManufacturerWestminster Pharmaceuticals, LLC
Substance NameBUPROPION HYDROCHLORIDE
Strength300
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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