Budesonide Inhalant
Product Images NDC 0487-9701

The text describes the mean change from baseline in nighttime asthma symptoms over a period of 12 weeks for a placebo group and two other treatment groups receiving different doses.*

This is a prescription medication in a 2mL unit-dose ampule used for inhalation only. It contains 0.25mg of micronized budesonide, which should be used immediately after opening in jet nebulizers only. The medication should be stored at 20°- 25°C (68°-77°F) and protected from light in a foil envelope placed upright in the carton. Instructions for use should be followed as directed by a physician. For further details, check the package insert or call customer service.*

This is a prescription medication with the NDC code 0487-9701-01. It is for inhalation only and comes in a plastic ampule with a 2 mL sterile suspension that contains 0.5 mg of micronized budesonide. The inactives include citric acid, edetate disodium dihydrate, polysorbate 80, sodium chloride, sodium citrate, and water for injection. The medication should be used as directed by a physician and the package insert should be reviewed for full prescribing information. Once opened, the contents of an ampule should be used immediately. It should be used only in a jet nebulizer and not in an ultrasonic nebulizer. The medication should be stored at controlled room temperature between 20-25°C (68-77°F) and should be protected from light. The medication is manufactured by a company called "Finetherapeutics" located in West Columbia, SC. The product should be kept out of reach of children.*

This text provides instructions for handling and using Budesonide inhalation suspension. The medication should be stored at room temperature and shaking the ampule before use is recommended. The medication is used with a nebulizer machine and the user should wear an appropriate mask to avoid getting mist in their eyes. Finally, the used ampule should be disposed of properly.*