Age About 2 Years Or Younger (Age Factor)
Sotalol Hydrochloride Tablet
Product Images NDC 72162-1932
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Sotalol Hydrochloride (NDC 72162-1932). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Bryant Ranch Prepack, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Figure 2 (Figure2)
The given text appears to provide information related to recurrence-free survival in a study comparing Oral Sotalol to Placebo. The text includes p-values for three different doses of Oral Sotalol (80 mg, 120 mg, and 160 mg) compared to the Placebo group. These p-values may indicate the statistical significance of the difference in recurrence-free survival between the different treatment groups.*
Figure 3 (Figure3)
Label (Lbl721621932)
This text appears to be the description of a medication called "Sotalol Hydrochloride Tablets, USP". The tablets contain 120 mg of Sotalol Hydrochloride, and the National Drug Code (NDC) for this medication is 72162-1932-1. It is advised to store the medication at a temperature between 20° and 25°C (68° to 77°F) and to keep it out of the reach of children. The medication should be dispensed in a tight, light-resistant container as per USP guidelines. It seems to have been manufactured by Oxford Pharmaceuticals LLC and relabeled by Bryant Ranch Prepack, Inc. The text does not provide any additional information.*
Molecular Structure (Molecularstructure)
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
