NDC 60219-1544
Hydroxychloroquine Sulfate 200 mg tablet, film coated
On the label: Amneal Pharmaceuticals.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Amneal Pharmaceuticals of New York, LLC | Brookhaven, NY, United States | Makes it, tests it, packages it and labels it | No problems foundSep 25, 2026 · 14 inspections |
Product details
- Generic drug
- Hydroxychloroquine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA210577
- On the market since
- May 17, 2018
- Package NDCs
60219-1544-1- Official label
- DailyMed (National Library of Medicine), updated Jun 11, 2024
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