NDC 71610-701
Hydroxychloroquine Sulfate 200 mg tablet
On the label: Aphena Pharma Solutions - Tennessee, Inc.. It's repackaged: Aphena Pharma Solutions - Tennessee, Inc. 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 |
Repackaging site
- Aphena Pharma Solutions - Tennessee, LLC, Cookeville, TN, United States · repackages it
Product details
- Generic drug
- Hydroxychloroquine: every company that makes it
- Form
- tablet, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA210441
- On the market since
- May 1, 2018
- Package NDCs
71610-701-5371610-701-80- Official label
- DailyMed (National Library of Medicine), updated May 1, 2023
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