Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 71335-3069

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 71335-3069). 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

Figure (Figure)

A forest plot showing results for subgroups in the MERIT-HF study. The plot compares total mortality, total mortality or all-cause hospitalization (time to first event), and total mortality or hospitalization for heart failure (time to first event) between metoprolol succinate extended-release tablets and placebo. It includes multiple subgroups such as geographic region, NYHA class, ejection fraction, ischemic etiology, sex, race, myocardial infarction history, diabetes, hypertension status, and heart rate, with relative risk and 95% confidence intervals depicted for each outcome.*

FDA Label Image

Label (Lbl713353069)

Metoprolol Succinate Extended-Release Tablets USP, 200 mg strength, labeled as 30 tablets. Package indicates each tablet contains 190 mg metoprolol succinate equivalent to 200 mg metoprolol tartrate. The product is repackaged by Bryant Ranch Prepack, Inc. and manufactured by Dr. Reddys Laboratories Ltd. Storage instructions and warnings are also present along with two QR codes for GTIN and package insert.*

FDA Label Image

Structure (Structure)

Chemical structure of metoprolol succinate, illustrating the molecular formula including the metoprolol moiety and the succinate component.*

* 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.