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WELLBUTRIN - bupropion hydrochloride

Navigation: NDC > Supplier starting with: G > GLAXOSMITHKLINE LLC
Field Value
NDC Code: 0173-0178
Proprietary Name: WELLBUTRIN
Suffix:
Non-Proprietary Name: bupropion hydrochloride
Dosage Form: TABLET, FILM COATED
Method: ORAL
Original Marketing Date: 21-06-1989
Category Name: NDA
Application Number: NDA018644
Labeler: GLAXOSMITHKLINE LLC
Substance Name: BUPROPION HYDROCHLORIDE
Active Numerator Strength: 100
Active Ingredient Unit: mg/1
Pharm Classes: Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]
DEA Schedule: