Ketorolac Tromethamine Injection, Solution
Product Images NDC 70518-3800

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 70518-3800). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Mm2 (Ketorolac Tromethamine 60mg 2ml (30mg mL) 70518 3800 01)

Mm2 (Ketorolac Tromethamine 60mg   2ml (30mg  mL) 70518 3800 01)
Label for ketorolac tromethamine injection solution, 30 mg/mL strength, with a quantity of 2 mL per vial. The label indicates intramuscular use only and single-dose vials. It is repackaged by RemedyRepack Inc., with manufacturing by Fosun Pharma USA Inc., Princeton, NJ. Includes an NDC number, barcode, and QR code.*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Ketorolac Tromethamine injection solution label displaying a concentration of 60 mg per 2 mL (30 mg/mL). The package contains 25 single-dose 2 mL vials intended for intramuscular use. The label shows that the product is repackaged by RemedyRepack Inc. and manufactured by Fosun Pharma USA Inc., Princeton, NJ. It includes usage instructions to protect from light and store at specified temperatures, with a barcode and QR code present.*
FDA Label Image

Ketorolac-structure (Ketorolac Structure)

Ketorolac-structure (Ketorolac Structure)
Chemical structure diagram of ketorolac tromethamine showing the molecular arrangement of its components, including the ketorolac moiety and 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.