NDC 68382-096
Hydroxychloroquine sulfate 200 mg tablet, film coated
On the label: Zydus Pharmaceuticals (USA) Inc..
Where it's 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 |
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
- Jan 3, 2008
- Package NDCs
68382-096-0168382-096-0568382-096-3068382-096-77- Official label
- DailyMed (National Library of Medicine), updated Dec 19, 2023
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