Metoprolol Succinate Tablet, Extended Release
Product Images NDC 71205-179

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 71205-179). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

Image-01 (Image 01)

Chemical structure diagram showing the molecular structure of Metoprolol Succinate, the active ingredient in the product Metoprolol Succinate 50 mg extended-release oral tablets by Proficient Rx LP.*

FDA Label Image

Image-02 (Image 02)

A forest plot chart titled 'Results for Subgroups in MERIT-HF' presenting relative risk and 95% confidence intervals across various subgroups. The chart compares Metoprolol Succinate Extended-Release Tablets versus placebo for three clinical outcomes: total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure. Subgroups include geographic region, NYHA class, ejection fraction, etiology, sex, race, myocardial infarction history, diabetes mellitus status, hypertension history, and heart rate categories.*

FDA Label Image

Image-03 (Image 03)

FDA Label Image

71205-179-90 (Image 05)

Metoprolol Succinate 50 mg extended-release tablets packaging label by Proficient Rx LP. The label indicates a quantity of 30 tablets, each containing 47.5 mg metoprolol succinate equivalent to 50 mg metoprolol tartrate. Tablets are white, round, biconvex, film-coated, engraved with "N/50", and scored on both sides. Manufactured by Novast Laboratories Ltd in Nantong, China. Storage instructions specify 20°-25°C (68°-77°F).*

* 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.