Moxifloxacin Solution/ Drops
Product Images NDC 65862-840

3 FDA label images from Aurobindo Pharma Limited · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Moxifloxacin (NDC 65862-840). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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

Package Label-principal Display Panel 0.5% (3 mL) Container Label (Moxifloxacin Fig1)

Package Label-principal Display Panel 0.5% (3 mL) Container Label (Moxifloxacin Fig1)
MOXIFLOXACIN Ophthalmic Solution USP 0.5% (5 mg/mL) in a 3 mL bottle label. The label states it is sterile and for topical ophthalmic use only. Distributed by Aurobindo Pharma USA, Inc., made in India, with NDC 65862-840-03 visible.*
FDA Label Image

Package Label-principal Display Panel 0.5% (3 mL) Carton Label (Moxifloxacin Fig2)

Package Label-principal Display Panel 0.5% (3 mL) Carton Label (Moxifloxacin Fig2)
Packaging label for Moxifloxacin Ophthalmic Solution USP 0.5%, a sterile eye drop solution supplied in a 3 mL container. The label indicates it is for topical ophthalmic use only, with each mL containing 5 mg of moxifloxacin. Distributed by Aurobindo Pharma USA, Inc., the label includes storage instructions and active/inactive ingredient details.*
FDA Label Image

Chemical Structure (Moxifloxacin Str)

Chemical Structure (Moxifloxacin Str)
Chemical structure of moxifloxacin, depicting its molecular arrangement with various functional groups and ring systems consistent with the fluoroquinolone class of antibiotics.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.