NDC 50090-6173
Bupropion hydrochloride (XL) 150 mg tablet, extended release
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Lannett Company, Inc.'s NDC 0527-2415.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hangzhou Minsheng Binjiang Pharmaceutical Co.,Ltd | Hangzhou, China | Makes it | Serious problems, FDA actionMar 7, 2025 · 6 inspections, 1 with FDA action |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · repackages it and relabels it
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, extended release
- Strength
- 150 mg
- Approval
- ANDA ANDA208652
- On the market since
- Jan 8, 2018
- Package NDCs
50090-6173-050090-6173-150090-6173-2- Official label
- DailyMed (National Library of Medicine), updated Oct 27, 2022
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