Latanoprost Solution/ Drops
Product Images NDC 65862-872

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 Latanoprost (NDC 65862-872). 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.

Product Images & Figures Index

FDA Label Image

Package Label-principal Display Panel (0.005% (125 mcg/2.5 mL))

Package Label-principal Display Panel (0.005% (125 mcg/2.5 mL))
Label for Latanoprost Ophthalmic Solution 0.005% (125 mcg/2.5 mL) by Aurobindo Pharma Limited. The label includes NDC 65862-872-25, indicates the product is sterile and for prescription use only, with dosing instructions for one drop in the affected eye(s) in the evening. Distributed by Aurobindo Pharma USA, Inc.*
FDA Label Image

Package Label-principal Display Panel (0.005% (125 mcg/2.5 mL))

Package Label-principal Display Panel (0.005% (125 mcg/2.5 mL))
The packaging label for Latanoprost Ophthalmic Solution 0.005% (125 mcg/2.5 mL), a sterile eye drop solution. The label shows a 2.5 mL bottle with directions to use one drop in the affected eye(s). It is manufactured by Aurobindo Pharma Limited and marked Rx only. Storage instructions recommend refrigeration before opening and protection from light.*
FDA Label Image

Latanoprost Chemical Structure (Latanoprost Str)

Latanoprost Chemical Structure (Latanoprost Str)
Chemical structure of Latanoprost showing its molecular framework with hydroxyl groups and ester functional groups, alongside the molecular weight value 432.58.*

* 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.