Metoprolol Succinate Tablet, Extended Release
Product Images NDC 71610-642

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 71610-642). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aphena Pharma Solutions - Tennessee, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Bottle Label 50 mg (71610 0642 45)

Bottle Label 50 mg (71610 0642 45)
Label for Metoprolol Succinate ER USP 50 mg extended release tablets, containing 45 tablets per bottle. Manufactured by Novast Laboratories Ltd., Nantong, China, and repackaged by Aphena Pharma, Cookeville, TN. Includes NDC number 71610-0642-45 and storage instructions at controlled room temperature. Marked RX Only.*
FDA Label Image

Aphena Pharma Solutions (TN)

Aphena Pharma Solutions (TN)
FDA Label Image

Image-01 (Image 01)

Image-01 (Image 01)
Chemical structure of Metoprolol Succinate showing the molecular arrangement of the active ingredient.*
FDA Label Image

Image-02 (Image 02)

Image-02 (Image 02)
A forest plot chart titled 'Results for Subgroups in MERIT-HF' showing relative risk and 95% confidence intervals for total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure. Data are grouped by patient characteristics such as region, NYHA class, ejection fraction, etiology, sex, race, previous myocardial infarction, diabetes mellitus, hypertension, and heart rate.*
FDA Label Image

Image-03 (Image 03)

Image-03 (Image 03)

* 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.