Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 72162-1857

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 72162-1857). 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

Label (Lbl721621857)

Label (Lbl721621857)
Label for Metoprolol Succinate Extended-Release Tablets USP, 50 mg, film-coated oral tablets. The package contains 100 tablets. The product is relabeled by Bryant Ranch Prepack, Inc., Burbank, CA, and manufactured by Alkem Laboratories Ltd. The label includes storage instructions and a warning to keep out of reach of children.*
FDA Label Image

Metoprolol-structure (Metoprolol Structure)

Metoprolol-structure (Metoprolol Structure)
Chemical structure diagram showing the molecular structure of Metoprolol Succinate, the active ingredient in Metoprolol Succinate ER Tablets. The structure includes the characteristic functional groups and components of the extended-release formulation.*
FDA Label Image

Metoprolol-table1a (Metoprolol Table1a)

Metoprolol-table1a (Metoprolol Table1a)
A forest plot chart illustrating relative risk and 95% confidence intervals for subgroups in the MERIT-HF study. The chart compares total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure outcomes between Metoprolol Succinate Extended-Release Tablets and placebo across various patient subgroups. The x-axis represents relative risk values from 0 to 2.*

* 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.