Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 50090-7239

View Photos of 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 50090-7239). 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.

Product Images & Figures Index

FDA Label Image

Figure (Figure)

Figure (Figure)
A forest plot chart titled "Results for Subgroups in MERIT-HF" displaying relative risk and 95% confidence intervals for total mortality, total mortality or all-cause hospitalization (time to first event), and total mortality or hospitalization for heart failure (time to first event). The chart compares results favoring metoprolol succinate extended-release tablets versus placebo across various subgroups including geographic location, NYHA class, ejection fraction, ischemic etiology, sex, race, prior myocardial infarction, diabetes status, hypertension history, and heart rate.*
FDA Label Image

Label Image (Lbl500907239)

Label Image (Lbl500907239)
Metoprolol succinate 50 mg extended-release film-coated tablets carton label. Contains 90 tablets. Each film-coated tablet has 50 mg metoprolol succinate equivalent to metoprolol tartrate. Manufactured by A-S Medication Solutions, Libertyville, IL 60048. Storage instructions specify 68 to 77 degrees Fahrenheit.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure diagram of Metoprolol succinate showing the molecular components and bonds of the active ingredient in the extended-release tablet form.*

* 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.