Product Images Wixela Inhub
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Product Label Images
The following 18 images provide visual information about the product associated with Wixela Inhub NDC 70518-2501 by Remedyrepack Inc., 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.
Wixela Inhub is an inhalation powder medication with the active ingredients Fluticasone Propionate and Salmeterol, which are used to treat asthma and chronic obstructive pulmonary disease (COPD). The package contains 60 doses at a strength of 250mcg/50 mcg. The medication is manufactured by Mylan in Morgantown, WV 26505, and repackaged by RemedyRepack Inc. in Indiana, PA 15701. The directions for use are specified in the package insert, and the medication should be stored at a temperature range of 20-26°C (63-77°F) with excursions permitted to 15-30°C (59-86°F) [See USP]. The expiration date and lot number are not available. It is advised to keep this and all medication out of the reach of children.*
This appears to be a combination of numerical values and text related to a drug treatment study. The text mentions "Fluicasone propionate" and "Saimeterol" being taken twice daily, and has a chart with weeks 0-12 and an endpoint. The rest of the text is mostly illegible due to formatting issues and errors.*
This appears to be data on the change in FEV (Forced Expiratory Volume) for different treatment groups on the first day of treatment. The treatment groups include Fluticasone propionate and Salmeterol inhaler, as well as a placebo group. The data includes the number of participants in each group and the dosage. However, the rest of the text is not-readable due to errors.*
This is a study evaluating the effect of Fluticasone Propionate and Salmeterol inhalation powder in improving lung function in patients with a baseline forced expiratory volume (FEV) of 1207 mL. The study had a placebo group and a group receiving Salmeterol alone. The results recorded the changes in FEV over 24 weeks with the inhalation powder group showing improvement in their lung function.*
The text is a table showing the change in forced expiratory volume (FEV) for patients receiving various treatments. The treatments include Fluticasone propionate and Salmeterol inhalation, Fluticasone propionate only, and a Placebo. The data includes the daily dose, with the endpoint of the study being between day 1 and week 24. The table also includes the number of patients (N) for each treatment group.*
* 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.