NDC 55154-3567
Hydroxychloroquine Sulfate 200 mg tablet, film coated
On the label: Cardinal Health 107, LLC. It's repackaged: Cardinal Health 107, LLC rebottles it from Dr. Reddy's Laboratories Inc.'s NDC 43598-721.
Where the pills inside were 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
55154-3567-0- Official label
- DailyMed (National Library of Medicine), updated Jun 3, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?