NDC 51655-098
Bupropion HydrochlorideXL 150 mg tablet, extended release
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals 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
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages 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
- Sep 6, 2022
- Package NDCs
51655-098-2651655-098-5251655-098-83- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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