NDC 68682-580
Bupropion Hydrobromide 174 mg tablet, extended release
On the label: Oceanside Pharmaceuticals..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bausch Health Companies Inc. | Steinbach, Canada | Makes it | No problems foundMay 19, 2023 · 6 inspections |
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 174 mg
- Approval
- NDA authorized generic NDA022108
- On the market since
- Jun 29, 2026
- Package NDCs
68682-580-30- Official label
- DailyMed (National Library of Medicine), updated Jun 1, 2026
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