NDC 57664-761
Hydroxychloroquine sulfate 200 mg tablet
On the label: Caraco Pharmaceutical Laboratories, Ltd..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ALKALOIDA Vegyeszeti Gyar zartkoruen mukodo Reszvenytarsasag | Tiszavasvari, Hungary | Makes it, tests it and packages it | Problems found, fixed voluntarilyMar 12, 2025 · 6 inspections |
Product details
- Generic drug
- Hydroxychloroquine: every company that makes it
- Form
- tablet, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA201691
- On the market since
- Jun 18, 2018
- Package NDCs
57664-761-1357664-761-88- Official label
- DailyMed (National Library of Medicine), updated Nov 11, 2022
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