NDC 76282-481
Bupropion Hydrochloride(XL) 300 mg tablet, extended release
On the label: Exelan Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| InvaGen Pharmaceuticals, Inc | Hauppauge, NY, United States | Makes it and tests it | No problems foundOct 25, 2023 · 18 inspections |
| InvaGen Pharmaceuticals, Inc | Central Islip, NY, United States | Tests it and packages it | Problems found, fixed voluntarilyJul 17, 2026 · 4 inspections |
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 300 mg
- Approval
- ANDA ANDA206556
- On the market since
- Jun 12, 2017
- Package NDCs
76282-481-0576282-481-3076282-481-90- Official label
- DailyMed (National Library of Medicine), updated Aug 1, 2023
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