NDC 50090-6871
Bupropion HydrochlorideSR 150 mg tablet, film coated, extended release
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions 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 |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · repackages it and relabels it
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 20, 2018
- Package NDCs
50090-6871-050090-6871-150090-6871-250090-6871-3- Official label
- DailyMed (National Library of Medicine), updated May 1, 2024
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