Ketorolac Tromethamine Solution/ Drops
Product Images NDC 47335-221

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Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Ketorolac Tromethamine (NDC 47335-221). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, Inc., 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

Ketorolac-structure (Ketorolac Structure)

FDA Label Image

Spl-ketorolac-carton-1 (Spl Ketorolac Carton 1)

Spl-ketorolac-carton-1 (Spl Ketorolac Carton 1)
This is an ophthalmic solution for use in the eyes only. The active ingredient is ketorolac tromethamine USP 0.5%. It also contains preservative and inactive ingredients. The usual dosage is one drop four times a day. Sun Pharmaceutical Industries is the distributor, and the product is manufactured in India. The package is not child-resistant, and it should be kept out of reach of children. It is not clear what the product is used for specifically.*
FDA Label Image

Spl-ketorolac-carton-2 (Spl Ketorolac Carton 2)

Spl-ketorolac-carton-2 (Spl Ketorolac Carton 2)
This is a prescription ophthalmic solution containing ketorolac tromethamine USP 0.5%. The solution is preserved with benzalkonium chloride solution (50%) NF 0.02%, and formulated with other inactive components including edetate disodium USP 0.1%, octoxynol 40, sodium chloride USP and hydrochloric acid NF and/or sodium hydroxide NF to adjust pH to 7.4. The recommended dosage is one drop four times a day. The solution should be kept at 20° to 25°C (68° to 77°F) and protected from light. This package is not child-resistant and should be kept away from children. The solution is manufactured and distributed by Sun Pharmaceutical Industries, Inc. The product has an NDC code of 47335-220-90.*
FDA Label Image

Spl-ketorolac-carton-3 (Spl Ketorolac Carton 3)

FDA Label Image

Spl-ketorolac-label-1 (Spl Ketorolac Label 1)

Spl-ketorolac-label-1 (Spl Ketorolac Label 1)
This is a description of an ophthalmic solution used only in the eyes, containing ketorolac tromethamine USP 0.5% and benzalkonium chloride solution (50%) NF 0.02% as a preservative. This solution is distributed by Sun Pharmaceutical Industries in Cranbury, NJ and manufactured by Sun Pharmaceutical Ind. Ltd, India. The usual dosage is one drop four times a day, and it should be protected from light. Batch number PJLB2345 188 with an expiry date of November 2014.*
FDA Label Image

Spl-ketorolac-label-2 (Spl Ketorolac Label 2)

Spl-ketorolac-label-2 (Spl Ketorolac Label 2)
This is an ophthalmic solution with the active ingredient ketorolac tromethamine USP 0.5%. It is manufactured by Sun Pharmaceutical Industries and comes in a 5ml package. The usual dosage is one drop four times a day, and the solution should be protected from light. The prescription should be used exclusively for the eyes. The text includes information on the ingredients, dosage, and manufacturer of the solution.*
FDA Label Image

Spl-ketorolac-label-3 (Spl Ketorolac Label 3)

Spl-ketorolac-label-3 (Spl Ketorolac Label 3)
This is an eye medication with the active ingredient ketorolac tromethamine. The medication comes in a 0.5% ophthalmic solution and is intended to be used four times a day. Specific dosing instructions can be found in the package insert. The medication should be protected from light. The NDC number is 47335-219-90 and it was manufactured by Sun Pharmaceutical Industries Ltd in India. The code "PULB233 155" and "Rx only" suggests that this is a prescription drug.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.