NDC 55154-8180
Bupropion Hydrochloride 75 mg tablet, film coated
On the label: Cardinal Health 107, LLC. It's repackaged: Cardinal Health 107, LLC rebottles it from BluePoint Laboratories.'s NDC 68001-308.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apotex Inc. | Etobicoke, Canada | Makes it and tests it | No problems foundSep 27, 2024 · 9 inspections, 1 with FDA action |
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 75 mg
- Approval
- ANDA ANDA076143
- On the market since
- Jan 29, 2018
- Package NDCs
55154-8180-0- Official label
- DailyMed (National Library of Medicine), updated Apr 24, 2026
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