Ketorolac Tromethamine
Product Images NDC 71872-7188

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Ketorolac Tromethamine (NDC 71872-7188). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Purchasing Solutions, Llc, 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

71872-7188-1.pdp (71872 7188 1)

Label for Ketorolac Tromethamine Injection USP 60 mg/2 mL (30 mg/mL), packaged as a 2 mL single-dose fliptop vial. The injectable is for intramuscular use only, with storage instructions at controlled room temperature 20 to 25°C (68 to 77°F). Manufactured by Hospira, Inc. and repackaged and distributed by Medical Purchasing Solutions, LLC, Scottsdale, AZ.*

FDA Label Image

Hospira Logo (Ketorolac Tromethamine 01)

FDA Label Image

Structural Formula Of Ketorolac (Ketorolac Tromethamine 02)

Chemical structure diagram showing Ketorolac Tromethamine, including its molecular formula components C15H13NO3 and C4H11NO3. The illustration depicts the molecular arrangement of atoms for the active ingredient Ketorolac Tromethamine.*

FDA Label Image

Hospira Logo (Ketorolac Tromethamine 03)

FDA Label Image

Hospira Logo (Ketorolac Tromethamine 04)

FDA Label Image

Principal Display Panel (2 mL Vial Label)

Label for Ketorolac Tromethamine injection USP 60 mg/2 mL single-dose fill. The label indicates a 2 mL vial for intramuscular use only, with the NDC 0409-3796-19. It is marked Rx only and shows Hospira, Inc. as the manufacturer located in Lake Forest, IL.*

* 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.