"0173-0135-55" National Drug Code (NDC)

Wellbutrin 60 TABLET, FILM COATED in 1 BOTTLE (0173-0135-55)
(GlaxoSmithKline LLC)

NDC Code0173-0135-55
Package Description60 TABLET, FILM COATED in 1 BOTTLE (0173-0135-55)
Product NDC0173-0135
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameWellbutrin
Proprietary Name SuffixSr
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19961115
Marketing Category NameNDA
Application NumberNDA020358
ManufacturerGlaxoSmithKline LLC
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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