Metoprolol Succinate
Product Images NDC 71335-2435

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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 71335-2435). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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 (Figure001)

Figure (Figure001)
This text provides information on the results of a study called MERIT-HF, focusing on the total mortality and hospitalization outcomes for heart failure patients treated with Wetoprolol Succinate Extended-Release tablets compared to a placebo. The study looked at various subgroups including NYHA class, ejection fraction, ischemic etiology, sex, race, previous medical history such as myocardial infarction, diabetes, and hypertension. It also includes mean heart rates for different subgroups. The study indicates favorable outcomes for Wetoprolol Succinate in certain subgroups. Key terms include US (United States), NYHA (New York Heart Association), EF (ejection fraction), and HR (heart rate).*
FDA Label Image

Label (Lbl713352435)

Label (Lbl713352435)
Each extended-release tablet contains 95 mg of Metoprolol Succinate equivalent to 100 mg of Metoprolol Tartrate, USP. This package is child-resistant and contains 30 tablets. It should be stored at 20° to 25°C (68° to 77°F) in a tight, light-resistant container. The tablets are only available by prescription and should be kept out of reach of children. For more information and details, visit https://dailymed.nlm.nih.gov/dailymed/*
FDA Label Image

Structure (Structure001)

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