NDC 85534-0069
Ciprofloxacin 250 mg tablet, film coated
On the label: Hawaii Repack, Inc.. It's repackaged: Hawaii Repack, Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-076.
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
- 250 mg
- Approval
- ANDA ANDA077859
- On the market since
- Apr 26, 2007
- Package NDCs
85534-0069-085534-0069-185534-0069-285534-0069-385534-0069-485534-0069-585534-0069-6- Official label
- DailyMed (National Library of Medicine), updated Jul 13, 2026
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