NDC 68071-3901
Ciprofloxacin 250 mg tablet
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Solco Healthcare U.S., LLC's NDC 43547-688.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Yiling Pharmaceutical Ltd | Shijiazhuang, China | Makes it | Serious problems, FDA actionOct 11, 2024 · 2 inspections, 1 with FDA action |
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · repackages it
Product details
- Generic drug
- Ciprofloxacin: every company that makes it
- Form
- tablet, oral
- Strength
- 250 mg
- Approval
- ANDA ANDA208921
- On the market since
- Oct 1, 2023
- Package NDCs
68071-3901-1- Official label
- DailyMed (National Library of Medicine), updated Oct 14, 2025
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