NDC 62135-876
Bupropion Hydrochloride (XL) 300 mg tablet, extended release
On the label: Chartwell RX, LLC..
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
- Aug 21, 2017
- Package NDCs
62135-876-30- Official label
- DailyMed (National Library of Medicine), updated Apr 5, 2024
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