Metoprolol Succinate
Product Images NDC 50090-5412

3 FDA label images from A-s Medication Solutions · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 50090-5412). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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

Figure (Fe222a69 B261 4e41 83ab Af76ee17812d 01)

Figure (Fe222a69 B261 4e41 83ab Af76ee17812d 01)
Chemical structure of metoprolol succinate showing the molecular arrangement including the aromatic ring, ether, hydroxyl, amine groups, and the succinate moiety.*
FDA Label Image

Figure (Fe222a69 B261 4e41 83ab Af76ee17812d 02)

Figure (Fe222a69 B261 4e41 83ab Af76ee17812d 02)
A forest plot showing results for subgroups in the MERIT-HF study. It compares the relative risk and 95% confidence intervals for total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure, favoring metoprolol succinate or placebo across various demographic and clinical subgroups.*
FDA Label Image

Label Image (Lbl500905412)

Label Image (Lbl500905412)
Metoprolol succinate 100 mg extended-release tablets label from A-S Medication Solutions. The label states that each film-coated extended-release tablet contains metoprolol succinate equivalent to 100 mg metoprolol tartrate. It includes storage instructions to store at 65 to 70 degrees Fahrenheit and specifies a package size of 90 extended-release tablets. The product NDC is 50090-5412.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.