Wellbutrin Sr 00173-0135
Generic: Bupropion Hydrochloride
Product NDC
00173-0135- Manufacturer
- Glaxosmithkline Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 15, 1996
- Listing Expires
- December 31, 2027
- Application
- NDA020358
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Bupropion Hydrochloride | 150 mg/1 |
Drug Class
Aminoketone [EPC]Dopamine Uptake Inhibitors [MoA]Increased Dopamine Activity [PE]
Packaging Options(1)
60 TABLET, FILM COATED in 1 BOTTLE (0173-0135-55)