NDC 60687-351
Bupropion Hydrochloride 100 mg tablet, film coated
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from BluePoint Laboratories.'s NDC 68001-309.
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 |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Recalls
- Dec 27, 2022 · Class II · Amerisource Health Services LLC
Failed Impurities/Degradation Specifications
Lots: Lot #: 1003837, Exp. Date 01/31/2023
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 100 mg
- Approval
- ANDA ANDA076143
- On the market since
- Feb 1, 2018
- Package NDCs
60687-351-0160687-351-11- Official label
- DailyMed (National Library of Medicine), updated Jun 24, 2026
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