Metoprolol Succinate
Product Images NDC 50090-6483

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 50090-6483). 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)

Figure (Aa40c17c D04a 4e23 Aaab 6283cb37ee24 01)
Chemical structure of metoprolol succinate, showing the molecular arrangement of the active ingredient metoprolol along with the succinate moiety.*
FDA Label Image

Figure (Aa40c17c D04a 4e23 Aaab 6283cb37ee24 02)

Figure (Aa40c17c D04a 4e23 Aaab 6283cb37ee24 02)
A forest plot chart titled 'Results for Subgroups in MERIT-HF' displaying relative risk and 95% confidence intervals for various subgroups comparing metoprolol succinate versus placebo. The chart has three sections assessing total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure. Subgroups include geographic region, NYHA class, ejection fraction, etiology, sex, race, myocardial infarction history, diabetes status, hypertension status, and heart rate. The plot shows markers and lines indicating risk ratios with labels explaining abbreviations.*
FDA Label Image

Label Image (Lbl500906483)

Label Image (Lbl500906483)
Metoprolol succinate extended release 100 mg tablets carton from A-S Medication Solutions. The label indicates each pill contains 100 mg metoprolol succinate equivalent to metoprolol tartrate. The package contains 30 tablets and instructs storage at 68 to 77 degrees Fahrenheit. The NDC number is 50090-6483-0.*

* 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.