NDC 70518-3063
Ciprofloxacin 500 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack 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 |
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
- Apr 2, 2021
- Package NDCs
70518-3063-070518-3063-170518-3063-270518-3063-370518-3063-470518-3063-570518-3063-6- Official label
- DailyMed (National Library of Medicine), updated Aug 3, 2026
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