"71335-1622-8" National Drug Code (NDC)

Bupropion 56 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1622-8)
(Bryant Ranch Prepack)

NDC Code71335-1622-8
Package Description56 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1622-8)
Product NDC71335-1622
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20141101
Marketing Category NameANDA
Application NumberANDA202304
ManufacturerBryant Ranch Prepack
Substance NameBUPROPION HYDROCHLORIDE
Strength150
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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