Product Images Ketorolac Tromethamine

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Product Label Images

The following 7 images provide visual information about the product associated with Ketorolac Tromethamine NDC 47335-220 by Sun Pharmaceutical Industries, Inc., such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

ketorolac-structure - ketorolac structure

ketorolac-structure - ketorolac structure

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.*

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.*

spl-Ketorolac-carton-3 - spl Ketorolac carton 3

spl-Ketorolac-carton-3 - spl Ketorolac carton 3

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.*

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.*

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.*

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.