NDC 70518-3573
Ofloxacin 3 mg per 1 mL solution/ drops
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Bausch & Lomb Incorporated's NDC 24208-434.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bausch & Lomb Incorporated | Tampa, FL, United States | Makes it, packages it and labels it | Serious problems, FDA actionMar 20, 2026 · 17 inspections, 3 with FDA action |
Product details
- Generic drug
- Ofloxacin: every company that makes it
- Form
- solution/ drops, ophthalmic
- Strength
- 3 mg per 1 mL
- Approval
- ANDA ANDA076622
- On the market since
- Nov 7, 2022
- Package NDCs
70518-3573-070518-3573-1- Official label
- DailyMed (National Library of Medicine), updated Aug 14, 2026
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