NDC 68180-120
Hydroxychloroquinesulfate 200 mg tablet, film coated
On the label: Lupin Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Chhatrapati Sambhajinagar, India | Makes it and packages it | Problems found, fixed voluntarilyMar 15, 2024 · 5 inspections |
Product details
- Generic drug
- Hydroxychloroquine: every company that makes it
- Form
- tablet, film coated
- Strength
- 200 mg
- Approval
- ANDA ANDA210543
- On the market since
- Jul 6, 2018
- Package NDCs
68180-120-0168180-120-02- Official label
- DailyMed (National Library of Medicine), updated Jul 6, 2018
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