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"67767-142-05" National Drug Code (NDC)

Bupropion Hydrochloride 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (67767-142-05)
(Actavis South Atlantic LLC)

NDC Code67767-142-05
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (67767-142-05)
Product NDC67767-142
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20100331
End Marketing Date20160930
Marketing Category NameANDA
Application NumberANDA077285
ManufacturerActavis South Atlantic 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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/67767-142-05





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