Bupropion Hydrobromide 68682-0581
Product NDC
68682-0581- Manufacturer
- Oceanside Pharmaceuticals
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 29, 2026
- Listing Expires
- December 31, 2027
- Application
- NDA022108
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Bupropion Hydrobromide | 348 mg/1 |
Drug Class
Aminoketone [EPC]Dopamine Uptake Inhibitors [MoA]Increased Dopamine Activity [PE]
Packaging Options(1)
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-581-30)