NDC 67046-1523
Hydroxychloroquine Sulfate 200 mg tablet, film coated
On the label: Coupler LLC. It's repackaged: Coupler LLC rebottles it from Ipca Laboratories Limited's NDC 83980-001.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Guardian Drug Company, Inc. | Dayton, NJ, United States | Makes it | No problems foundJan 16, 2026 · 9 inspections |
| Ipca Laboratories Limited | Silvassa, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyApr 26, 2023 · 5 inspections, 2 with FDA action |
| Ipca Laboratories Limited | Dhar, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJun 23, 2023 · 4 inspections, 1 with FDA action |
Repackaging site
- Coupler LLC, West Chester, PA, United States · repackages it
Product details
- Generic drug
- Hydroxychloroquine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA040766
- On the market since
- Feb 24, 2025
- Package NDCs
67046-1523-3- Official label
- DailyMed (National Library of Medicine), updated Feb 24, 2025
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