NDC 83008-082
Bupropion Hydrochloride (XL) 150 mg tablet, film coated, extended release
On the label: Lake Erie Medical DBA Quality Care Products LLC. It's repackaged: Lake Erie Medical DBA Quality Care Products LLC rebottles it from ScieGen Pharmaceuticals, Inc.'s NDC 50228-144.
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
- Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC, Location not on file · relabels it
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA207479
- On the market since
- Aug 28, 2024
- Package NDCs
83008-082-30- Official label
- DailyMed (National Library of Medicine), updated Dec 19, 2024
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