NDC 76420-929
Ciprofloxacin 500 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Solco Healthcare U.S., LLC's NDC 43547-689.
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
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Ciprofloxacin: every company that makes it
- Form
- tablet, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA208921
- On the market since
- Oct 1, 2023
- Package NDCs
76420-929-0176420-929-0576420-929-1476420-929-2076420-929-3076420-929-6076420-929-90- Official label
- DailyMed (National Library of Medicine), updated Jun 26, 2026
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