NDC 72789-065
Ciprofloxacin 500 mg tablet, film coated
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Carlsbad Technology, Inc.'s NDC 61442-223.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Carlsbad Technology, Inc. | Carlsbad, CA, United States | Makes it and tests it | Problems found, fixed voluntarilyJun 30, 2026 · 12 inspections |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Ciprofloxacin: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA076126
- On the market since
- Oct 10, 2009
- Package NDCs
72789-065-20- Official label
- DailyMed (National Library of Medicine), updated Oct 15, 2026
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