Ipratropium Bromide And Albuterol Sulfate Solution
Product Images NDC 71205-051
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Product Visual Gallery
This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Ipratropium Bromide And Albuterol Sulfate (NDC 71205-051). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Proficient Rx Lp, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Product Images & Figures Index
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This document provides data on adverse events that occurred in over 1% of patients in at least one treatment group, where the combination treatment resulted in the highest percentage. The table shows the number of patients and percentage of patients that experienced adverse events, broken down by body system and specific condition. Adverse events are reported for treatment with Albuterol, Ipratropium, and Ipratropium Bromide.*
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This is a description of a relabeled Ipratropium Bromide / Albuterol Sulfate inhalation solution manufactured by Nephron Pharmaceuticals Corporation. It comes in a 15mL package with 5 vials of 3mL each. The solution is for oral inhalation only, and each vial contains 0.5 mg ipratropium bromide and 3 mg albuterol sulfate. It has a product ID of S1005115 and a GTIN of 0371205051150. The relabeling was done by Proficient Rx LP, located in Thousand Oaks, CA. The expiration date is not specified, but it is recommended to store the medication between 2° and 25°C (36° and 77°F) and keep it out of the reach of children.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.