Ammonia N 13 Injection, Solution
Product Images NDC 52670-552

2 FDA label images from Mayo Clinic · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ammonia N 13 (NDC 52670-552). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mayo Clinic, 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
Ammonia N 13 Injection Usp Is Provided As A Ready To Use Sterile, Pyrogen-free, Clear And Colorless Solution. Each mL Of The Solution Contains Between 0.138 Gbq To 1.387 Gbq (3.75 Mci To 37.5mci) Of [13n] Ammonia, At The End Of Synthesis (eos), In 0.9% Aqueous Sodium Chloride. The Ph Of The Solution Is Between 4.5 To 7.5. The Recommended Dose Of Radioactivity (0.368-0.736 Gbq, 10-20 Mci) Is Associated With A Theoretical Mass Dose Of 0.5-1.0 Picomoles (8.47-16.94 (Ammonia N 13 Usp 01)
Chemical structure diagram of ammonia N-13, showing the nitrogen atom labeled with isotope 13 bonded to three hydrogen atoms.*
FDA Label Image

Principal Display Panelndc 52670-552-30ammonia N13 Injection Uspintravenous Use Rx Only (Ammonia N 13 Usp 02)

Principal Display Panelndc 52670-552-30ammonia N13 Injection Uspintravenous Use Rx Only (Ammonia N 13 Usp 02)
Ammonia N 13 Injection USP label for intravenous use, Rx only. Contains sterile, non-pyrogenic solution with 0.9% sodium chloride. The label shows radioactive caution and details for activity, volume, concentration, and expiration times, with storage instructions at controlled room temperature. Manufactured by Mayo Clinic FET Radiochemistry Facility, Rochester, MN.*

* 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.