Bupropion Hydrochloride 68788-7988
Product NDC
68788-7988- Manufacturer
- Preferred Pharmaceuticals Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 6, 2021
- Listing Expires
- December 31, 2027
- Application
- ANDA076143
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Bupropion Hydrochloride | 100 mg/1 |
Drug Class
Aminoketone [EPC]Dopamine Uptake Inhibitors [MoA]Increased Dopamine Activity [PE]
Packaging Options(4)
100 TABLET, FILM COATED in 1 BOTTLE (68788-7988-1)
30 TABLET, FILM COATED in 1 BOTTLE (68788-7988-3)
60 TABLET, FILM COATED in 1 BOTTLE (68788-7988-6)
90 TABLET, FILM COATED in 1 BOTTLE (68788-7988-9)