Metoprolol Succinate Tablet, Extended Release
Product Images NDC 68071-3943

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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 68071-3943). 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 3943 1)

Pdp (68071 3943 1)
This is a product label for Metoprolol Succinate 50mg extended-release tablets by NuCare Pharmaceuticals, Inc. The tablets contain 47.5mg of Metoprolol Succinate equivalent to 50mg of Metoprolol Tartrate, USP. The NDC number for this product is 68071-3943-01. It is important to follow storage instructions, which recommend keeping the product at a controlled temperature of 68-77°F and keeping it out of reach of children. For more information, refer to the manufacturer's label and contact NuCare Pharmaceuticals, Inc. if needed.*
FDA Label Image

Figure (Figure001)

Figure (Figure001)
This text provides information on a study (MERIT-HF) comparing the effects of Metoprolol Succinate extended-release tablets versus a placebo on total mortality and hospitalization for heart failure in different subgroups. The results include data on various factors such as EF (ejection fraction), ischemic etiology, previous medical conditions (MI, diabetes mellitus, hypertension), demographics (sex, race), and heart rate. The study also mentions the definitions for abbreviations used, such as US (United States), NYHA (New York Heart Association), EF, and HR.*
FDA Label Image

Structure (Structure001)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.