NDC 70518-4056
Bupropion HydrochlorideSR 150 mg tablet, film coated, extended release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-175.
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 |
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA205794
- On the market since
- Apr 19, 2024
- Package NDCs
70518-4056-070518-4056-1- Official label
- DailyMed (National Library of Medicine), updated Oct 19, 2026
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