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"0187-0731-30" National Drug Code (NDC)

Wellbutrin 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-0731-30)
(Bausch Health US LLC)

NDC Code0187-0731-30
Package Description30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0187-0731-30)
Product NDC0187-0731
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameWellbutrin
Proprietary Name SuffixXl
Non-Proprietary NameBupropion Hydrochloride
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20030829
Marketing Category NameNDA
Application NumberNDA021515
ManufacturerBausch Health US LLC
Substance NameBUPROPION HYDROCHLORIDE
Strength300
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/0187-0731-30





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