Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 71335-2835

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 71335-2835). 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 (Lbl713352835)

Label for Metoprolol Succinate Extended-Release Tablets, USP, 50 mg strength. The label shows the NDC number 71335-2835-1 and indicates the product is relabeled by Bryant Ranch Prepack, Inc., Burbank, CA and manufactured by Alkem Laboratories Ltd. It states the package contains 100 tablets and provides storage instructions, caution, and a warning to keep out of reach of children.*

FDA Label Image

Metoprolol-structure (Metoprolol Structure)

Chemical structure of metoprolol succinate, illustrating the molecular arrangement of the active ingredient in Metoprolol Succinate ER Tablets 50 mg by Bryant Ranch Prepack.*

FDA Label Image

Metoprolol-table1a (Metoprolol Table1a)

A figure titled 'Results for Subgroups in MERIT-HF' presenting three forest plots comparing Metoprolol Succinate Extended-Release Tablets versus placebo across various patient subgroups. The plots display relative risk and 95% confidence intervals for Total Mortality, Total Mortality or All-Cause Hospitalization, and Total Mortality or Hospitalization for Heart Failure. Subgroups include geographic region, NYHA class, ejection fraction categories, ischemic etiology, sex, race, prior myocardial infarction, diabetes status, hypertension status, and heart rate categories.*

* 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.