Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 71335-9753

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 71335-9753). 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 (Lbl713359753)

Metoprolol Succinate Extended-Release Tablets USP 50 mg film-coated tablets, supplied in a package of 30 tablets. The label shows the NDC number 71335-9753-1 and indicates repackaging by Bryant Ranch Prepack, Inc. and manufacturing by Alkem Laboratories Ltd. Storage instructions and caution to keep out of reach of children are also present.*

FDA Label Image

Metoprolol-structure (Metoprolol Structure)

Chemical structure diagram of Metoprolol Succinate, showing the molecular arrangement of atoms including phenyl ring, hydroxyl groups, amine, and succinate moieties. The structure represents the extended-release formulation of metoprolol succinate tablets.*

FDA Label Image

Metoprolol-table1a (Metoprolol Table1a)

A forest plot showing results for subgroups in the MERIT-HF study. The chart compares relative risk and 95% confidence intervals for total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure, contrasting Metoprolol Succinate Extended-Release Tablets versus placebo across multiple patient subgroups.*

* 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.