Chemical Structure Of Fludeoxyglucose F 18 (Fludeoxyglucose F 18 Injection Usp 01)
Fludeoxyglucose F 18
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This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Fludeoxyglucose F 18 (NDC 76376-618). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Hamamatsu/queen�s Pet Imaging Center, 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.
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Principal Display Panelndc# 76376-618-3030 mL Multiple-dose Vialfludeoxyglucose F 18 Injection, Usp (Fludeoxyglucose F 18 Injection Usp 02)
Fludeoxyglucose F 18 Injection, USP is a diagnostic solution that is used for intravenous injection only. It comes in a 30mL multiple-use vial with a concentration range of 10-100 mCi/mL at the end of synthesis, and it has a shelf life of 12 hours after the end of synthesis. The solution is sterile, non-pyrogenic, and contains deoxy-2 [18F] fluoro-D-glucose 0.37–37.0 GBq (10-100 mCi) of no barrier added 2-deoxy-2-[18F]fluoro-D-glucose at EOS, [72 meq of citrate ions. It should be stored at 25°C (77°F) with excursions allowed to 15-30°C (56-86°F) according to USP controlled room temperature. It must be stored upright in a shielded container, and doses should be handled and withdrawn aseptically. The solution has a half-life of 109.7 minutes, and the manufacturer is Hamamatsu/Queen's Pet Imaging Center located in Honolulu, HI. Patients should not be given the solution if it contains particulate matter, and correct dosage calculations should be made from the calibration date and time.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
