NDC 70518-4214
Ciprofloxacin 500 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Aurobindo Pharma Limited's NDC 59651-867.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Product details
- Generic drug
- Ciprofloxacin: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 500 mg
- Approval
- ANDA ANDA077859
- On the market since
- Oct 15, 2024
- Package NDCs
70518-4214-070518-4214-170518-4214-270518-4214-3- Official label
- DailyMed (National Library of Medicine), updated Aug 31, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?