NDC 68788-7793
Bupropion HydrochlorideSR 200 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 50228-176.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ScieGen Pharmaceuticals, INC. | Hauppauge, NY, United States | Makes it and tests 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
- 200 mg
- Approval
- ANDA ANDA205794
- On the market since
- Oct 13, 2020
- Package NDCs
68788-7793-168788-7793-268788-7793-368788-7793-668788-7793-868788-7793-9- Official label
- DailyMed (National Library of Medicine), updated Mar 23, 2026
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