Metoprolol Succinate
Product Images NDC 50090-6486

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 50090-6486). 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 (Aa40c17c D04a 4e23 Aaab 6283cb37ee24 01)

Chemical structure of metoprolol succinate showing the molecular arrangement of its active ingredient components with functional groups including aromatic ring, alcohol, ether, amine, and carboxylic acid moieties.*

FDA Label Image

Figure (Aa40c17c D04a 4e23 Aaab 6283cb37ee24 02)

A forest plot illustrating results for subgroups in the MERIT-HF study, comparing metoprolol succinate versus placebo. The chart displays relative risk and 95% confidence intervals for total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure across various subgroups such as geographic location, NYHA class, ejection fraction, etiology, sex, race, history of myocardial infarction, diabetes, hypertension, and heart rate.*

FDA Label Image

Label Image (Lbl500906486)

Metoprolol succinate extended-release 25 mg tablets packaging label from A-S Medication Solutions. The label indicates each film-coated extended-release tablet contains metoprolol succinate equivalent to 25 mg metoprolol tartrate. Package includes 30 tablets, with storage instructions to keep at 68 to 77 degrees Fahrenheit. Package NDC is 50090-6486-0.*

* 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.