Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 51655-193

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 51655-193). 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 193 26)

Label for Metoprolol Succinate Extended-Release Tablets, USP 100 mg, oral film-coated tablets, extended-release. The package contains 90 tablets. Labeler is Northwind Health Company, LLC. The label includes storage instructions, dosage note to see package insert, and various regulatory details including NDC 51655-193-26.*

FDA Label Image

2 (Image 5)

Chemical structure of metoprolol succinate, showing its molecular arrangement including aromatic ring, ether linkages, and succinate moiety.*

FDA Label Image

1 (Image 6)

A forest plot chart showing results for subgroups in the MERIT-HF study, comparing the relative risk and 95% confidence intervals for total mortality, total mortality or all-cause hospitalization, and total mortality hospitalization for heart failure. The chart lists various subgroups (e.g., US, non-US, NYHA classes, ejection fraction levels) and displays risk estimates favoring either metoprolol succinate extended-release or placebo across three clinical outcomes.*

FDA Label Image

1 (Image 9)

The image shows a white, oblong extended-release film-coated tablet of metoprolol succinate 100 mg. There are no visible markings, imprints, or scoring on the tablet surface. The tablet is intended for oral use and is labeled under Northwind Health Company, LLC.*

* 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.