Ketorolac Tromethamine
Product Images NDC 50436-6190

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 50436-6190). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unit Dose Services, 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

Image Description (50436 6190 2)

Image Description (50436 6190 2)
Packaging label for Ketorolac Tromethamine 10 mg oral tablets, containing 20 tablets. The label indicates the drug name, dosage strength, quantity, and manufacturer information, including Teva Pharmaceuticals in Parsippany, NJ. Storage and dosage instructions are partially visible, along with sections for lot number and expiration date, and the label specifies the product is RX only.*
FDA Label Image

Image Description (50436 6190 3)

Image Description (50436 6190 3)
Ketorolac Tromethamine 10 mg film-coated tablets in a package of 30 tablets. The label indicates the active ingredient Ketorolac Tromethamine USP with a typical dosage of one tablet every 4 to 6 hours. The product is labeled for manufacturing by Teva Pharmaceuticals and distributed by Unit Dose Services, LLC. The label includes storage instructions and regulatory information.*
FDA Label Image

Ketorolac Tromethamine Structural Formula (Ketorolac Tromethamine Tablet Film Coated A074754 1)

Ketorolac Tromethamine Structural Formula (Ketorolac Tromethamine Tablet Film Coated A074754 1)
Chemical structure diagram of Ketorolac Tromethamine showing the ketorolac molecule linked with the tromethamine moiety.*

* 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.