Moxifloxacin Solution/ Drops
Product Images NDC 67296-2348

3 FDA label images from Redpharm Drug · 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 67296-2348). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

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

Product Images & Figures Index

FDA Label Image

Chemical Structure (Moxifloxacin Str)

Chemical Structure (Moxifloxacin Str)
Chemical structure of moxifloxacin, showing its molecular formula with fluorine (F), chlorine ion (Cl-), and various functional groups including ketones and hydroxyl groups. The structure includes a cyclopropyl group and methoxy substituent characteristic of the compound.*
FDA Label Image

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

Package Label-principal Display Panel 0.5% (3 mL) Cantainer Label (Moxifloxacin Fig1)
Moxifloxacin Ophthalmic Solution 0.5%, 3 mL sterile eye drops packaging label. The label shows the drug is for topical ophthalmic use with a concentration of 5 mg/mL of moxifloxacin hydrochloride USP. Manufactured for Northstar Rx LLC, Memphis, TN, and produced in India. Storage instructions indicate keeping it between 2° to 25°C (36° to 77°F).*
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)
Label for Moxifloxacin Ophthalmic Solution, USP 0.5%, sterile, 3 mL, an eye drop product. The label includes directions for topical ophthalmic use only, active ingredient strength, inactive ingredients, usual dosage instructions, storage conditions, manufacturer information (Eugia Pharma Specialities Limited, India), and Northstar branding. The NDC 16714-643-01 appears on the label, indicating product identification.*

* 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.