NDC 16571-112
Hydroxychloroquine Sulfate 200 mg tablet, film coated
On the label: Rising Pharma Holdings, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Laurus Labs Limited | Anakapalli, India | Makes it and tests it | Problems found, fixed voluntarilyFeb 10, 2023 · 2 inspections |
Product details
- Generic drug
- Hydroxychloroquine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA210959
- On the market since
- May 29, 2023
- Package NDCs
16571-112-0116571-112-0616571-112-1016571-112-50- Official label
- DailyMed (National Library of Medicine), updated May 6, 2024
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