NDC 50090-4747
Bupropion Hydrochloride 150 mg tablet, extended release
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-319.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Salcette, India | Makes it and packages it | Problems found, fixed voluntarilyNov 21, 2025 · 9 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, extended release, oral
- Strength
- 150 mg
- Approval
- ANDA ANDA090693
- On the market since
- Jun 14, 2017
- Package NDCs
50090-4747-050090-4747-150090-4747-2- Official label
- DailyMed (National Library of Medicine), updated Feb 6, 2026
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