Moxifloxacin Hydrochloride Tablet, Film Coated
Product Images NDC 70518-3738

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Moxifloxacin Hydrochloride (NDC 70518-3738). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Remedy_label (Remedy Label)

This is a prescription drug named Moxifloxacin, produced by Aurobindo Pharma in Dayton, NJ. It comes in a tablet form of 400 mg and is packaged with 7 tablets per quantity. The medication should be kept away from children and should not be used with alcohol or nonprescribed drugs without consulting a medical provider. The package insert should be consulted for usage instructions and the drug should be stored at 20-25°C (88-77°F), with excursions permitted up to 15-30°C (59-86°F) [See USP]. There is a lot number and source NDC available, but the expiration date is not provided. The drug has been repackaged by RemedyRepack Inc., Indiana, PA 15701.*

FDA Label Image

Figure 1 (Moxifloxacin Fig1)

FDA Label Image

Structure (Moxifloxacin Str)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.