NDC 70518-4081
Bupropion hydrochloride 150 mg tablet, extended release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-067.
Where the pills inside were 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
- 150 mg
- Approval
- ANDA ANDA216800
- On the market since
- May 16, 2024
- Package NDCs
70518-4081-070518-4081-170518-4081-270518-4081-370518-4081-4- Official label
- DailyMed (National Library of Medicine), updated Aug 27, 2026
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