NDC 50228-338
Bupropion Hydrochloride(SR) 150 mg tablet, film coated, extended release
On the label: ScieGen Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ScieGen Pharmaceuticals, INC. | Hauppauge, NY, United States | Makes it and labels it | Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action |
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA206122
- On the market since
- May 1, 2019
- Package NDCs
50228-338-1150228-338-3150228-338-61- Official label
- DailyMed (National Library of Medicine), updated Mar 8, 2022
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