NDC 68071-2912
Hydroxychloroquine sulfate 200 mg tablet, film coated
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare 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
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Hydroxychloroquine: every company that makes it
- Form
- tablet, film coated
- Strength
- 200 mg
- Approval
- ANDA ANDA040657
- On the market since
- Jan 3, 2008
- Package NDCs
68071-2912-268071-2912-368071-2912-9- Official label
- DailyMed (National Library of Medicine), updated Nov 20, 2023
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