NDC 71335-2329
Moxifloxacin Hydrochloride 400 mg tablet, film coated
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Aurobindo Pharma Limited's NDC 65862-603.
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
- Bryant Ranch Prepack, Burbank, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Moxifloxacin: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 400 mg
- Approval
- ANDA ANDA202632
- On the market since
- Mar 4, 2014
- Package NDCs
71335-2329-171335-2329-2- Official label
- DailyMed (National Library of Medicine), updated Feb 2, 2026
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