NDC 43598-721
Hydroxychloroquine Sulfate 200 mg tablet, film coated
On the label: Dr. Reddy's Laboratories Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Appco Pharma LLC | Piscataway, NJ, United States | Makes it, tests it and packages it | Problems found, fixed voluntarilyMay 14, 2026 · 9 inspections |
| Axxelent Pharma Science Private Limited | Tirupati, India | Makes it, tests it and packages it | Not inspected on record |
Product details
- Generic drug
- Hydroxychloroquine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA210441
- On the market since
- May 1, 2018
- Package NDCs
43598-721-0143598-721-05- Official label
- DailyMed (National Library of Medicine), updated Dec 5, 2025
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