NDC 72789-108
Ciprofloxacin 500 mg tablet, film coated
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Hikma Pharmaceuticals USA Inc.'s NDC 0143-9928.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hikma Pharmaceuticals LLC | Amman, Jordan | Makes it | Problems found, fixed voluntarilySep 5, 2019 · 5 inspections |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Recalls
- Feb 6, 2013 · Class II · West-ward Pharmaceutical Corp.
Presence of Foreign Substance(s): A complaint was received for a rubber-like material in a 500 mg Ciprofloxacin tablet.
Lots: Lot #: CB222A, Exp 06/16
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Ciprofloxacin: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA076558
- On the market since
- Jun 9, 2004
- Package NDCs
72789-108-0272789-108-1072789-108-1472789-108-2072789-108-2872789-108-30- Official label
- DailyMed (National Library of Medicine), updated Mar 19, 2026
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