Metoprolol Succinate
Product Images NDC 71335-3096

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 71335-3096). 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 (Lbl713353096)

Label (Lbl713353096)
Metoprolol succinate extended-release tablets USP 200 mg with 30 tablets per package. Label includes NDC 71335-3096-1 and states repackaged by Bryant Ranch Prepack, Inc. in Burbank, CA, and manufactured by Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd. The label shows storage instructions and warnings about medication safety.*
FDA Label Image

Structure (Metaprolol 01)

Structure (Metaprolol 01)
Chemical structure of metoprolol succinate, showing the molecular arrangement of metoprolol with succinate ions, as depicted in the image associated with the Bryant Ranch Prepack product.*
FDA Label Image

Figure (Metaprolol 02)

Figure (Metaprolol 02)
A forest plot titled 'Results for Subgroups in MERIT-HF' depicting relative risk and 95% confidence intervals for total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure. The data is stratified by various subgroups, including geographic location, NYHA class, ejection fraction, ischemic etiology, sex, race, myocardial infarction history, diabetes status, hypertension history, and heart rate. The plot compares outcomes favoring metoprolol succinate extended-release tablets versus placebo.*

* 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.