NDC 67296-1764
Moxifloxacin 5 mg per 1 mL solution/ drops
On the label: RedPharm Drug. Inc.. It's repackaged: RedPharm Drug. Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-840.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apitoria Pharma Private Limited | Sangareddy, India | Makes the active ingredient and tests it | Problems found, fixed voluntarilySep 27, 2024 · 6 inspections |
| Eugia Pharma Specialities Limited | Sangareddy, India | Makes it, tests it and packages it | Serious problems, FDA actionFeb 6, 2026 · 7 inspections, 2 with FDA action |
Repackaging site
- RedPharm Drug, Eden Prairie, MN, United States · repackages it
Recalls
- Jan 14, 2022 · Class II · Aurobindo Pharma USA Inc.
Failed Impurities/Degradation Specifications
Lots: Lot#: CMF210001, CMF210003, CMF210004, Exp 6/2023 - Dec 2, 2019 · Class III · AuroMedics Pharma LLC
Discoloration: Market complaints of discoloration in Moxifloxacin Ophthalmic Solution.
Lots: Lot #s: CMF190008; CMF190009, Exp. 04/2021; CMF190025; CMF190026, Exp. 06/2021.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Moxifloxacin: every company that makes it
- Form
- solution/ drops
- Strength
- 5 mg per 1 mL
- Approval
- ANDA ANDA206242
- On the market since
- Oct 4, 2017
- Package NDCs
67296-1764-3- Official label
- DailyMed (National Library of Medicine), updated Jul 25, 2024
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