"42806-349-05" National Drug Code (NDC)

Bupropion Hydrochloride 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-349-05)
(Epic Pharma, LLC)

NDC Code42806-349-05
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42806-349-05)
Product NDC42806-349
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
ManufacturerEpic Pharma, 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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