NDC 67296-1616
Moxifloxacin Hydrochloride 400 mg tablet, film coated
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 57237-156.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 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
- tablet, film coated
- Strength
- 400 mg
- Approval
- ANDA ANDA202632
- On the market since
- Jan 1, 2018
- Package NDCs
67296-1616-5- Official label
- DailyMed (National Library of Medicine), updated Jan 21, 2022
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