NDC 0527-2430
Bupropion hydrochloride (XL) 300 mg tablet, extended release
On the label: Lannett Company, 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
- 300 mg
- Approval
- ANDA ANDA208652
- On the market since
- Jan 8, 2018
- Package NDCs
0527-2430-320527-2430-410527-2430-430527-2430-46- Official label
- DailyMed (National Library of Medicine), updated Dec 31, 2025
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