NDC 60687-782
Bupropion Hydrochloride XL 150 mg tablet, extended release
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-319.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Salcette, India | Makes it and packages it | Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Recalls
- Jun 24, 2024 · Class II · Amerisource Health Services LLC
Failed Dissolution Specifications; the product is dissolving faster than the specified limits.
Lots: Lot 1017343, Exp. 12/31/2025
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, extended release, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA090693
- On the market since
- Jan 15, 2024
- Package NDCs
60687-782-0160687-782-11- Official label
- DailyMed (National Library of Medicine), updated Aug 31, 2026
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