NDC 70518-3738
Moxifloxacin Hydrochloride 400 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. 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 |
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
- May 30, 2023
- Package NDCs
70518-3738-0- Official label
- DailyMed (National Library of Medicine), updated May 18, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?