Ketorolac Tromethamine Solution/ Drops
Product Images NDC 47335-219

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Ketorolac Tromethamine (NDC 47335-219). 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)

Chemical structure of ketorolac tromethamine, showing the ketorolac moiety and the tromethamine component represented as a molecular diagram with connected atoms and functional groups.*

FDA Label Image

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

Carton label for Ketorolac Tromethamine Ophthalmic Solution 0.5%, an eye drop solution. The label shows Rx only 3 mL packaging, NDC 47335-219-90, and states 'For use in the eyes only.' It includes manufacturer information for Sun Pharmaceutical Industries, Inc. and distribution details. The label also lists active and inactive ingredients, preservative, and storage instructions.*

FDA Label Image

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

Label for Ketorolac Tromethamine Ophthalmic Solution 0.5%, an eye drop solution in a 5 mL package. The label includes the NDC 47335-220-90, details for USE IN THE EYES ONLY, and directions stating Rx only. It is distributed and manufactured by Sun Pharmaceutical Industries, Inc. The label lists active ingredient strength and preservatives.*

FDA Label Image

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

Label for Ketorolac Tromethamine Ophthalmic Solution 0.5%, an eye drop solution. The label indicates Rx only and a 10 mL bottle size. It lists Sun Pharmaceutical Industries, Inc. as the distributor and Sun Pharmaceutical Industries Ltd. as the manufacturer, noting the product is for ophthalmic use only. The label includes storage and usage instructions and a barcode.*

FDA Label Image

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

Label for Ketorolac Tromethamine Ophthalmic Solution 0.5%, a 10 mL solution/drops product. The label includes active ingredient ketorolac tromethamine USP 0.5%, preservative benzalkonium chloride solution 0.02%, and directions for use in the eyes only. Distributed by Sun Pharmaceutical Industries, Inc., Cranbury, NJ, and manufactured by Sun Pharmaceutical Ind. Ltd., India.*

FDA Label Image

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

Label for Ketorolac Tromethamine Ophthalmic Solution 0.5%, a prescription eye drop solution distributed by Sun Pharmaceutical Industries, Inc. and manufactured by Sun Pharmaceutical Ind. Ltd, India. The 5 mL label includes active ingredient concentration, preservative information, usage instructions, and regulatory details including NDC and bar code.*

FDA Label Image

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

Label for Ketorolac Tromethamine Ophthalmic Solution 0.5% (5 mg/mL) in a 3 mL dosage form. The label lists the active ingredient ketorolac tromethamine USP 0.5%, preservative benzalkonium chloride solution (0.02%), and usage instructions mentioning one drop four times a day. Distributed by Sun Pharmaceutical Industries, Inc. and manufactured by Sun Pharmaceutical Ind. Ltd in India. Includes NDC 47335-219-90 and a barcode.*

* 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.