NDC 83301-0024
Bupropion Hydrochloride (XL) 150 mg tablet, extended release
On the label: Mullan Pharmaceutical Inc..
Where it's 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 |
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA208652
- On the market since
- Jun 17, 2024
- Package NDCs
83301-0024-183301-0024-283301-0024-383301-0024-4- Official label
- DailyMed (National Library of Medicine), updated Jan 29, 2026
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