Moxifloxacin Ophthalmic Solution Solution/ Drops
Product Images NDC 68083-210

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Moxifloxacin Ophthalmic Solution (NDC 68083-210). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gland 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

Moxifloxacin-bottle-label (Moxifloxacin Bottle Label)

Label for Moxifloxacin Ophthalmic Solution, USP 0.5% (5 mg/mL) in a 3 mL sterile solution for topical ophthalmic use only. The label includes storage instructions (2°C to 25°C), NDC number 68083-210-01, dosage guidance to read the enclosed insert, and the manufacturer Gland Pharma Limited in India. There is a barcode and space for lot and expiration information.*

FDA Label Image

Moxifloxacin-carton-label (Moxifloxacin Carton Label)

The packaging label for Moxifloxacin Ophthalmic Solution, USP 0.5% (5 mg/mL) shows a 3 mL ophthalmic solution for topical use only. The label includes the active ingredient moxifloxacin hydrochloride equivalent to 5 mg moxifloxacin per mL. It is manufactured by Gland Pharma Limited in Hyderabad, India. The label specifies sterile, Rx only, and proper storage at 2°C to 25°C (36°F to 77°F). The NDC number 68083-210-01 appears prominently on the panels.*

FDA Label Image

Moxifloxacin-structure (Moxifloxacin Structure)

Chemical structure of Moxifloxacin, the active ingredient in Moxifloxacin Ophthalmic Solution 5 mg/mL by Gland Pharma Limited. The structure displays its molecular arrangement including fluorine, oxygen, nitrogen atoms, and characteristic ring systems.*

* 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.