Iophendylate Injection
» Iophendylate Injection is sterile Iophendylate.
Packaging and storage— Preserve in single-dose containers, preferably of Type I glass, protected from light.
Bacterial endotoxins 85 It contains not more than 0.9 USP Endotoxin Unit per mg of iophendylate.
Other requirements— It conforms to the Definition, responds to the Identification test, and meets the requirements for Specific gravity, Refractive index, Residue on ignition, Free acids, Free iodine, Saponification value, and Assay under Iophendylate. It meets also the requirements under Injections 1.
Auxiliary Information— Please check for your question in the FAQs before contacting USP.
Topic/Question Contact Expert Committee
Monograph Ian DeVeau, Ph.D.
Director, Veterinary Drugs and Radiopharmaceuticals
(RMI05) Radiopharmaceuticals and Medical Imaging Agents 05
Reference Standards Lili Wang, Technical Services Scientist
85 Radhakrishna S Tirumalai, Ph.D.
Senior Scientist
(MSA05) Microbiology and Sterility Assurance
USP32–NF27 Page 2671