Metoprolol Succinate Tablet, Extended Release
Product Images NDC 68071-2522

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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 68071-2522). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare Pharmaceuticals,inc., 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

Pdp (68071 2522 1)

Pdp (68071 2522 1)
Label for Metoprolol Succinate 50 mg extended-release tablets by NuCare Pharmaceuticals, Inc. The label shows an NDC 68071-2522-1 and indicates a pack size of 100 E-R tablets. It states each tablet contains 47.5 mg metoprolol succinate equivalent to 50 mg metoprolol tartrate and includes manufacturer and storage information.*
FDA Label Image

Figure (Fe222a69 B261 4e41 83ab Af76ee17812d 01)

Figure (Fe222a69 B261 4e41 83ab Af76ee17812d 01)
Chemical structure diagram of metoprolol succinate, showing the molecular arrangement of its compound components as represented in the image.*
FDA Label Image

Figure (Fe222a69 B261 4e41 83ab Af76ee17812d 02)

Figure (Fe222a69 B261 4e41 83ab Af76ee17812d 02)
A forest plot titled 'Results for Subgroups in MERIT-HF' showing the relative risk and 95% confidence intervals for total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure. The plot compares metoprolol succinate versus placebo across various subgroups such as geography, NYHA class, ejection fraction, ischemic etiology, sex, race, prior myocardial infarction, diabetes status, hypertension status, and heart rate. Columns indicate favoring metoprolol succinate or placebo with markers and confidence intervals for each subgroup.*

* 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.