NDC 70518-0859
Bupropion Hydrochloride 150 mg tablet, extended release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. 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 |
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, extended release
- Strength
- 150 mg
- Approval
- ANDA ANDA090693
- On the market since
- Nov 20, 2017
- Package NDCs
70518-0859-070518-0859-1- Official label
- DailyMed (National Library of Medicine), updated Jun 2, 2025
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