U.S. License Holder:
Draximage
Date of License:
December-30-1987
Last Update:
Nov-15-2024
FDA-Approved Indications
DRAXIMAGE MAA ((kit for the preparation of technetium Tc 99m albumin aggregated) injection), after radiolabeling with sodium pertechnetate Tc 99m, is a radioactive diagnostic agent indicated for:
Lung scintigraphy as an adjunct in the evaluation of pulmonary perfusion in adults and pediatric patients;
Peritoneovenous shunt scintigraphy as an aid in the evaluation of its patency in adults.