NDC 70518-4014
Bupropion HydrochlorideXL 300 mg tablet, extended release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Epic Pharma, LLC's NDC 42806-416.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Yichang Humanwell Oral Solid Dosage Plant | Yichang, China | Makes it | No problems foundJul 21, 2023 · 2 inspections |
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 300 mg
- Approval
- ANDA ANDA210015
- On the market since
- Feb 7, 2024
- Package NDCs
70518-4014-070518-4014-1- Official label
- DailyMed (National Library of Medicine), updated Jun 12, 2026
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