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"0173-0722-00" National Drug Code (NDC)

Wellbutrin 60 TABLET, FILM COATED in 1 BOTTLE (0173-0722-00)
(GlaxoSmithKline LLC)

NDC Code0173-0722-00
Package Description60 TABLET, FILM COATED in 1 BOTTLE (0173-0722-00)
Product NDC0173-0722
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameWellbutrin
Proprietary Name SuffixSr
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20020625
Marketing Category NameNDA
Application NumberNDA020358
ManufacturerGlaxoSmithKline 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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0173-0722-00





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