Sotalol Hydrochloride Tablet
Product Images NDC 72789-137

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Sotalol Hydrochloride (NDC 72789-137). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx Pharmaceuticals, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

72789135 Label (72789135)

72789135 Label (72789135)
This is a medication containing Sotalol Hydrochloride. Each tablet has 160 mg. It is recommended to check usual dosage on the package insert. It should be stored in a light-resistant container, within controlled temperature conditions. It is marketed and packaged by PD-Rx Pharmaceuticals and manufactured by Oxford Pharmaceuticals. The bottle contains 100 tablets. The product's expiration date is 04/2022 and the LOT number is J20A35.*
FDA Label Image

72789136 Label (72789136)

72789136 Label (72789136)
Each tablet contains Sotalol Hydrochloride USP at a strength of 240 mg. It is manufactured by Oxford Pharmaceuticals and marketed by PD-Rx Pharmaceuticals, Inc. The product comes in a bottle containing 100 tablets and should be stored in a cool, dry place. The standard dosage should be referred to by consulting the package insert. Other details, such as GTIN, LOT, and SNO codes are also available.*
FDA Label Image

72789137 Label (72789137)

72789137 Label (72789137)
Each tablet contains 80mg of Sotalol Hydrochloride, manufactured by Oxford Pharmaceuticals LLC and marketed by PD-Rx Pharmaceuticals Inc. The tablets should be stored at a controlled temperature of 20° to 25°C (68° to 77°F). The usual dosage is to be determined by following the instructions given in the package insert. The product comes in a pack of 100 tablets and is identified by a GTIN of 00372789137018 and other identification numbers.*
FDA Label Image

72789138 Label (72789138)

72789138 Label (72789138)
Each tablet contains 120 mg of Sotalol Hydrochloride, indicated for the treatment of heart rhythm disorders. The tablets are packaged in a tight and light-resistant container and must be stored at a controlled room temperature. The usual dosage information is available in the package insert. The product is manufactured by PD-Rx Pharmaceuticals, Inc and packaged by Oxford Pharmaceuticals, LLC. The product is available in a bottle containing 100 tablets. The NDC number is 72789-138-01, and the expiration date is 04/2022.*
FDA Label Image

Age About 2 Years Or Younger (Age Factor)

FDA Label Image

Figure 2 (Figure2)

Figure 2 (Figure2)
The text shows the p-values indicating the comparison of recurrence-free survival between oral Sotalol and Placebo for different dosages. The numbers represent the different dosages and the corresponding p-values: 80mg-0325, 120mg-0018, 160mg-0029. No other information is available to provide further context.*
FDA Label Image

Figure 3 (Figure3)

FDA Label Image

Molecular Structure (Molecularstructure)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.