NDC 71335-3079
Hydroxychloroquine Sulfate 200 mg tablet, film coated
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Ipca Laboratories Limited's NDC 83980-001.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Guardian Drug Company, Inc. | Dayton, NJ, United States | Makes it | No problems foundJan 16, 2026 · 9 inspections |
| Ipca Laboratories Limited | Silvassa, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyApr 26, 2023 · 5 inspections, 2 with FDA action |
| Ipca Laboratories Limited | Dhar, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJun 23, 2023 · 4 inspections, 1 with FDA action |
Repackaging site
- Bryant Ranch Prepack, Burbank, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Hydroxychloroquine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA040766
- On the market since
- Jun 3, 2024
- Package NDCs
71335-3079-171335-3079-271335-3079-371335-3079-471335-3079-571335-3079-671335-3079-771335-3079-871335-3079-9- Official label
- DailyMed (National Library of Medicine), updated Feb 13, 2026
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