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Utilizing a suitable sterile automated compounding device or dispensing pin for accuracy, aseptically transfer the 10 mL dose into a plastic or glass bottle containing at least 500 to 1,000 mL intravenous parenteral nutrition solution containing dextrose or saline

A diagnostic-use formulation (0.05 mg base per ampule, for evaluating the pituitary's capacity to secrete growth hormone) was approved December 28, 1990 under NDA 19-863

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It may also be used as a dispensing container for diluent use

AOD9604 RCT summary and clinical efficacy Annals of Clinical and Laboratory Science (PubMed) Effect of intraarticular AOD9604 with hyaluronic acid in rabbit osteoarthritis model DrugBank AOD9604 drug summary