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.
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.
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 1-301-816-8178 |
(RMI05) Radiopharmaceuticals and Medical Imaging Agents 05 |
| Reference Standards | Lili Wang, Technical Services Scientist 1-301-816-8129 RSTech@usp.org |
|
| 85 |
Radhakrishna S Tirumalai, Ph.D.
Senior Scientist 1-301-816-8339 |
(MSA05) Microbiology and Sterility Assurance |
USP32–NF27 Page 2671