WELLBUTRIN - bupropion hydrochloride
Navigation: NDC > Supplier starting with: G > GLAXOSMITHKLINE LLC| Field | Value |
|---|---|
| NDC Code: | 0173-0135 |
| Proprietary Name: | WELLBUTRIN |
| Suffix: | SR |
| Non-Proprietary Name: | bupropion hydrochloride |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 15-11-1996 |
| Category Name: | NDA |
| Application Number: | NDA020358 |
| Labeler: | GLAXOSMITHKLINE LLC |
| Substance Name: | BUPROPION HYDROCHLORIDE |
| Active Numerator Strength: | 150 |
| 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: |