NDC 68071-3496
Bupropion Hydrochloride 300 mg tablet, extended release
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-320.
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
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, extended release
- Strength
- 300 mg
- Approval
- ANDA ANDA090693
- On the market since
- Jun 14, 2017
- Package NDCs
68071-3496-3- Official label
- DailyMed (National Library of Medicine), updated Aug 29, 2023
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