Ketorolac Tromethamine Solution/ Drops
Product Images NDC 65862-770

View Photos of 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 Ketorolac Tromethamine (NDC 65862-770). 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% (5 mL))

Package Label-principal Display Panel (0.5% (5 mL))
Label for Ketorolac Tromethamine Ophthalmic Solution 0.5%, 5 mL, a sterile eye drop solution for topical application in the eye. The label shows it is a prescription drug distributed by Aurobindo Pharma USA, Inc., made in India. It includes storage instructions to protect from light, bottle fill information, and space for lot and expiration dates.*
FDA Label Image

Package Label-principal Display Panel (0.5% (5 mL))

Package Label-principal Display Panel (0.5% (5 mL))
The image shows the unfolded carton label for Ketorolac Tromethamine 0.5% ophthalmic solution by Aurobindo Pharma Limited. The label states the 5 mL solution is for topical eye application, sterile, and Rx only. It includes active and inactive ingredients, storage conditions, and distributor information (Aurobindo Pharma USA, Inc.). The NDC 65862-770-05 and barcode are visible.*
FDA Label Image

Checmial-structure (Ketorolac Str)

Checmial-structure (Ketorolac Str)
Chemical structure diagram of Ketorolac Tromethamine, showing the molecular structure of the active ingredient Ketorolac Tromethamine as indicated by the product data.*

* 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.