NDC 31722-068
Bupropion hydrochloride 200 mg tablet, extended release
On the label: Camber Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Annora Pharma Private Limited | Sangareddy, India | Makes it and tests it | Problems found, fixed voluntarilyMar 28, 2025 · 4 inspections |
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA216800
- On the market since
- May 31, 2023
- Package NDCs
31722-068-0131722-068-0531722-068-6031722-068-90- Official label
- DailyMed (National Library of Medicine), updated Mar 23, 2026
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