NDC 67296-2232
Moxifloxacin Hydrochloride 5 mg per 1 mL solution/ drops
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Somerset Therapeutics, LLC's NDC 70069-081.
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 |
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Product details
- Generic drug
- Moxifloxacin: every company that makes it
- Form
- solution/ drops, ophthalmic
- Strength
- 5 mg per 1 mL
- Approval
- ANDA ANDA209698
- On the market since
- Nov 25, 2024
- Package NDCs
67296-2232-3- Official label
- DailyMed (National Library of Medicine), updated May 15, 2026
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