NDC 68788-4172
Bupropion Hydrochloride(XL) 300 mg tablet, film coated, extended release
On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-145.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ScieGen Pharmaceuticals, INC. | Hauppauge, NY, United States | Makes it, tests it and labels it | Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action |
Repackaging site
- Preferred Pharmaceuticals Inc., Anaheim, CA, United States · repackages it
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 300 mg
- Approval
- ANDA ANDA207479
- On the market since
- Jul 24, 2026
- Package NDCs
68788-4172-168788-4172-368788-4172-668788-4172-868788-4172-9- Official label
- DailyMed (National Library of Medicine), updated Jul 24, 2026
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