NDC 70518-4381
polymyxin b sulfate and trimethoprim sulfate 1 mg per 1 mL / 10000 [iU] per 1 mL solution/ drops
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Somerset Therapeutics, LLC's NDC 70069-311.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Somerset Therapeutics Private Limited | Bengaluru, India | Makes it, tests it, packages it and labels it | Serious problems, FDA actionFeb 21, 2025 · 10 inspections, 4 with FDA action |
Product details
- Generic drug
- Polymyxin B and Trimethoprim: every company that makes it
- Form
- solution/ drops, ophthalmic
- Strength
- 1 mg per 1 mL / 10000 [iU] per 1 mL
- Approval
- ANDA ANDA211572
- On the market since
- Jul 1, 2025
- Package NDCs
70518-4381-0- Official label
- DailyMed (National Library of Medicine), updated Sep 9, 2026
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