Bausch & Lomb Incorporated
Tampa, FL, United States · makes it, packages it and labels it
Serious problems, FDA action Last FDA inspection Mar 20, 2026. 17 inspections on record, 3 with serious problems.
NDC 50436-6112
Ofloxacin 3 mg per 1 mL solution/ drops
On the label: Unit Dose Services.
It's a repackaged product: Unit Dose Services rebottles it from Bausch & Lomb Incorporated's NDC 24208-434.
Where the pills inside were made
Repackaging site
- Unit Dose Services, · repackages it and relabels it
Product details
- Generic drug
- Ofloxacin: see every company that makes it
- Form
- solution/ drops
- Strength
- 3 mg per 1 mL
- Approval
- ANDA ANDA076622
- On the market since
- May 14, 2004
- Package NDCs
50436-6112-0- Official label
- DailyMed (National Library of Medicine), updated Mar 6, 2017
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