Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 71335-2834

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 71335-2834). 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 (Lbl713352834)

Label (Lbl713352834)
This packaging label is for Metoprolol Succinate Extended-Release Tablets USP, 25 mg strength. The label indicates 500 tablets per package. It is relabeled by Bryant Ranch Prepack, Inc., and manufactured by Alkem Laboratories Ltd. The label includes NDC 71335-2834-1, dosage form as film-coated, and instructions to store at controlled room temperature.*
FDA Label Image

Metoprolol-structure (Metoprolol Structure)

Metoprolol-structure (Metoprolol Structure)
Chemical structure of Metoprolol Succinate, showing the molecular arrangement including hydroxyl, methoxy, and amine functional groups, along with the succinate moiety.*
FDA Label Image

Metoprolol-table1a (Metoprolol Table1a)

Metoprolol-table1a (Metoprolol Table1a)
A forest plot chart illustrating relative risk and 95% confidence intervals for subgroups in the MERIT-HF study. The chart compares Metoprolol Succinate Extended-Release Tablets versus placebo across three outcomes: total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure. Subgroups include demographics, ejection fraction, etiology, sex, race, medical history, diabetes status, hypertension status, and heart rate ranges.*

* 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.