1. Home
  2. Labeler Index
  3. American Health Packaging
  4. 60687-524
  5. Product Images: Budesonide Inhalation

Product Images Budesonide Inhalation

View Photos of Packaging, Labels & Appearance

Product Label Images

The following 9 images provide visual information about the product associated with Budesonide Inhalation NDC 60687-524 by American Health Packaging, such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

Carton

Carton

This is a product description for a medication called Budesonide Inhalation Suspension. It comes in a box containing 30x2mL unit-dose ampules, each in a foil pouch. The lot/exp number is not readable. The medication is intended for prescription use only. The instructions on how to use this medication are provided but are not readable in this text.*

Figure 1

Figure 1

The text describes a chart or table showing the change in nighttime asthma from baseline for different doses of a medication over a period of 12 weeks. The medication is dosed at 0.25 mg, 0.5 mg, and 1.0 mg once daily. The chart shows p-values for each dose, with the lowest p-value (indicating statistical significance) being for the 0.25 mg dose at 0.001.*

Figure 2

Figure 2

Nighttime Asthma Change from Baseline data is shown in the given text. However, due to incorrect reading, the information is not entirely reliable and may not be useful.*

Figure 3

Figure 3

This appears to be a table or chart showing the mean change from baseline in nighttime asthma symptoms over a 12 week period, with data for different dosages of a drug or placebo. P-values for each dosage are also provided.*

Foil

Foil

Budesonide inhalation suspension is a prescription medicine that contains 0.5 mg of budesonide in each 2 mL of sterile suspension delivered by a dose amped for inhalation only. The usual dosage is directed by a medical professional and should be followed by patients. Detailed instructions are available in the package insert. The medicine should be stored at a controlled room temperature of 20°-25°C (58°-77°F), with excursions permitted between 1 to 30°C (59"-86°F) as stated by the United States Pharmacopeia (USP). Once the foil pouch of unopened ampule is opened, use the ampule within the two weeks. The package contains one unit dose ampule per pouch. Inactive ingredients include anhydrous citric acid, disodium edetate dihydrate, polysorbate 80, sodium chloride, and water for injection. This medicine is manufactured by LUPIN PHAR and distributed by American Health Packaging in Columbus, Ohio. Keep the medicine, along with other drugs, out of children's reach.*

IFU Figure 2

IFU Figure 2

IFU Figure 3

IFU Figure 3

IFU Figure 4

IFU Figure 4

Structure

Structure

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.