Metoprolol Succinate Tablet, Extended Release
Product Images NDC 63187-768

3 FDA label images from Proficient Rx Lp · 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 63187-768). 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

63187-768-30 (Container3)

63187-768-30 (Container3)
Label for Metoprolol Succinate 100 mg extended-release tablets by Proficient Rx LP. The label shows NDC 63187-768-30 and states each film-coated tablet contains 95 mg metoprolol succinate equivalent to 100 mg metoprolol tartrate. It includes packaging and product ID details, manufacturer Dr. Reddy's Laboratories Limited, and storage instructions.*
FDA Label Image

Figure (Figure)

Figure (Figure)
A forest plot showing the results for subgroups in the MERIT-HF study, comparing total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure between metoprolol succinate extended-release tablets and placebo. The plot includes subgroups by region, NYHA classification, ejection fraction, ischemic etiology, sex, race, history of myocardial infarction, diabetes, hypertension, and heart rate, with relative risk and 95% confidence intervals shown for each subgroup.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure diagram of Metoprolol succinate, showing the molecular arrangement of its active ingredient and succinate moiety.*

* 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.