Metoprolol Succinate
Product Images NDC 53002-1612

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 53002-1612). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rpk 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

Figure (Figure)

A forest plot titled 'Results for Subgroups in MERIT-HF' showing relative risk and 95% confidence intervals for total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure across various subgroups. Subgroups include geographic location, NYHA class, ejection fraction, etiology, sex, race, history of myocardial infarction, diabetes mellitus, hypertension, and heart rate categories. Each outcome compares metoprolol succinate extended-release tablets versus placebo.*

FDA Label Image

Label Image (Lbl530021612)

Metoprolol succinate 50 mg extended-release tablets packaging label from RPK Pharmaceuticals, Inc. The label indicates the product is supplied as 100 tablets with instructions to take 1 tablet daily with a meal or as directed. It displays dosage strength, product NDC (53002-1612), lot number, expiration date, and placeholders for clinic name, patient name, and prescribing information.*

FDA Label Image

Structure (Structure)

Chemical structure diagram of metoprolol succinate, showing the molecular arrangement of the active ingredient metoprolol succinate used in the product Metoprolol succinate by RPK Pharmaceuticals, Inc.*

* 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.