NDC 70518-4218
Bupropion Hydrochloride 100 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Alembic Pharmaceuticals Inc.'s NDC 62332-127.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Alembic Pharmaceuticals Limited | Panchmahal, India | Makes it | No problems foundJul 26, 2024 · 8 inspections |
Product details
- Generic drug
- Bupropion: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 100 mg
- Approval
- ANDA ANDA203013
- On the market since
- Oct 21, 2024
- Package NDCs
70518-4218-070518-4218-1- Official label
- DailyMed (National Library of Medicine), updated Jan 8, 2026
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