Ketorolac Tromethamine Solution/ Drops
Product Images NDC 65145-139

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Ketorolac Tromethamine (NDC 65145-139). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Caplin Steriles 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

Ketorolac-tromethamine-10ml-carton (Ketorolac Tromethamine 10ml Carton)

Ketorolac-tromethamine-10ml-carton (Ketorolac Tromethamine 10ml Carton)
Packaging label for Ketorolac Tromethamine Ophthalmic Solution 0.5%, sterile eye drops in a 10 mL bottle. The label states it is for topical ophthalmic use only, Rx only, and includes storage instructions. The labeler is Caplin Steriles Limited, India.*
FDA Label Image

Ketorolac-tromethamine-10ml-container (Ketorolac Tromethamine 10ml Container)

Ketorolac-tromethamine-10ml-container (Ketorolac Tromethamine 10ml Container)
Label for Ketorolac Tromethamine Ophthalmic Solution 0.5%, a 10 mL sterile eye drop solution by Caplin Steriles Limited. The label states the product is for topical ophthalmic use only and contains 0.5% ketorolac tromethamine active ingredient with benzalkonium chloride preservative. It includes storage instructions and dosage guidance.*
FDA Label Image

Ketorolac-tromethamine-3ml-carton (Ketorolac Tromethamine 3ml Carton)

Ketorolac-tromethamine-3ml-carton (Ketorolac Tromethamine 3ml Carton)
Packaging label for Ketorolac Tromethamine Ophthalmic Solution 0.5%, sterile 3 mL drops by Caplin Steriles Limited. The label states it is for topical ophthalmic use only and includes storage instructions, active and inactive ingredients, and manufacturer information with a barcode. The label also highlights usual dosage instructions and cautions to keep out of reach of children.*
FDA Label Image

Ketorolac-tromethamine-3ml-container (Ketorolac Tromethamine 3ml Container)

Ketorolac-tromethamine-3ml-container (Ketorolac Tromethamine 3ml Container)
Label for Ketorolac Tromethamine Ophthalmic Solution 0.5%, a sterile eye drop solution. The 3 mL bottle contains ketorolac tromethamine at 5 mg/mL concentration, with benzalkonium chloride as a preservative. Manufactured by Caplin Steriles Limited, India, for topical ophthalmic use only.*
FDA Label Image

Ketorolac-tromethamine-5ml-carton (Ketorolac Tromethamine 5ml Carton)

Ketorolac-tromethamine-5ml-carton (Ketorolac Tromethamine 5ml Carton)
carton for Ketorolac Tromethamine Ophthalmic Solution 0.5%, sterile 5 mL bottle, manufactured by Caplin Steriles Limited. The label states usage is for topical ophthalmic use only, includes active ingredient ketorolac tromethamine 0.5%, and preservatives. Provides storage instructions, dosage guidance, and manufacturer details with barcode and NDC number 65145-139-01.*
FDA Label Image

Ketorolac-tromethamine-5ml-container (Ketorolac Tromethamine 5ml Container)

Ketorolac-tromethamine-5ml-container (Ketorolac Tromethamine 5ml Container)
Label for Ketorolac Tromethamine Ophthalmic Solution 0.5% in a 5 mL sterile ophthalmic solution bottle. The label states it is for topical ophthalmic use only and lists ketorolac tromethamine 0.5% as the active ingredient and benzalkonium chloride 0.01% as a preservative. The product is manufactured by Caplin Steriles Limited, India.*
FDA Label Image

Ketorolac-tromethamine-structure (Ketorolac Tromethamine Structure)

Ketorolac-tromethamine-structure (Ketorolac Tromethamine Structure)
Chemical structure of Ketorolac Tromethamine, showing the molecular arrangement including a benzoyl group attached to a pyrrolizine ring with a carboxyl group, and the tromethamine moiety represented with its amino and hydroxymethyl groups.*

* 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.