Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 51655-519

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 51655-519). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, Llc, 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

Label (51655 519 26)

Label (51655 519 26)
Label for metoprolol succinate extended-release tablets, USP, 50 mg strength. The container holds 90 tablets. The label includes storage instructions to keep at controlled room temperature (15-30°C) and out of children's reach. It lists Northwind Pharmaceuticals USA, Inc. as the repackager and Northwind Health Company, LLC as the labeler. The NDC number is 51655-519-26.*
FDA Label Image

Image (Image 10)

Image (Image 10)
metoprolol succinate 50 mg extended release film-coated oral tablets in a blister pack. The image shows a strip with individual tablets sealed in transparent blister compartments. The labeler is Northwind Health Company, LLC.*
FDA Label Image

2 (Image 5)

2 (Image 5)
Chemical structure depicting metoprolol succinate, showing the molecular arrangement of the metoprolol moiety and the succinate component as a salt form.*
FDA Label Image

1 (Image 6)

1 (Image 6)
A forest plot chart titled 'Results for Subgroups in MERIT-HF' illustrating relative risk and 95% confidence intervals for three outcomes: Total Mortality, Total Mortality or All-Cause Hospitalization, and Total Mortality Hospitalization for Heart Failure. The plot compares metoprolol succinate extended-release versus placebo across various subgroups such as geographic region, NYHA class, ejection fraction, etiology, sex, race, myocardial infarction history, diabetes, hypertension, and heart rate.*

* 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.