Bupropion Hydrochloride 60505-0157
Product NDC
60505-0157- Manufacturer
- Apotex Corp
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 17, 2006
- Listing Expires
- December 31, 2026
- 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(5)
100 TABLET, FILM COATED in 1 BOTTLE (60505-0157-1)
30 TABLET, FILM COATED in 1 BOTTLE (60505-0157-3)
500 TABLET, FILM COATED in 1 BOTTLE (60505-0157-5)
1000 TABLET, FILM COATED in 1 BOTTLE (60505-0157-7)
90 TABLET, FILM COATED in 1 BOTTLE (60505-0157-9)