"23155-191-10" National Drug Code (NDC)

Bupropion Hydrochloride 1000 TABLET in 1 BOTTLE (23155-191-10)
(Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.)

NDC Code23155-191-10
Package Description1000 TABLET in 1 BOTTLE (23155-191-10)
Product NDC23155-191
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBupropion Hydrochloride
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20160819
Marketing Category NameANDA
Application NumberANDA206975
ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Substance NameBUPROPION HYDROCHLORIDE
Strength75
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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