"67767-135-60" National Drug Code (NDC)

Bupropion Hydrochloride 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67767-135-60)
(Actavis South Atlantic LLC)

NDC Code67767-135-60
Package Description60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67767-135-60)
Product NDC67767-135
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20100719
Marketing Category NameANDA
Application NumberANDA077455
ManufacturerActavis South Atlantic LLC
Substance NameBUPROPION HYDROCHLORIDE
Strength200
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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