"71335-1192-7" National Drug Code (NDC)

Bupropion Hydrochloride 21 TABLET in 1 BOTTLE (71335-1192-7)
(Bryant Ranch Prepack)

NDC Code71335-1192-7
Package Description21 TABLET in 1 BOTTLE (71335-1192-7)
Product NDC71335-1192
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20160819
Marketing Category NameANDA
Application NumberANDA206975
ManufacturerBryant Ranch Prepack
Substance NameBUPROPION HYDROCHLORIDE
Strength100
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/71335-1192-7