NDC 68788-7747
Hydroxychloroquine sulfate 200 mg tablet, film coated
On the label: Preferred Pharmaceuticals, Inc... It's repackaged: Preferred Pharmaceuticals, Inc.. rebottles it from Zydus Pharmaceuticals (USA) Inc.'s NDC 68382-096.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action |
| Zydus Lifesciences Limited | Solan, India | Makes it and tests it | No problems foundMar 9, 2020 · 6 inspections |
Repackaging site
- Preferred Pharmaceuticals Inc., Anaheim, CA, United States · repackages it
Product details
- Generic drug
- Hydroxychloroquine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA040657
- On the market since
- Jul 1, 2020
- Package NDCs
68788-7747-268788-7747-3- Official label
- DailyMed (National Library of Medicine), updated May 11, 2026
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