Metoprolol Succinate
Product Images NDC 21695-950

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 21695-950). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rebel Distributors Corp, 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

Structural Formula For Metoprolol Succinate (44a4e8de 0430 48f8 8178 093afcded438 01)

Chemical structure showing the molecular arrangement of metoprolol succinate, depicting the aromatic ring, side chains, and succinate moiety as part of the compound's formula.*

FDA Label Image

Results For Subgroups In Mertit-hf (44a4e8de 0430 48f8 8178 093afcded438 02)

A forest plot chart displaying results for subgroups in the MERIT-HF study comparing metoprolol succinate extended release tablets versus placebo. The chart shows relative risk and 95% confidence intervals for total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure, stratified by demographic and clinical subgroups such as NYHA class, ejection fraction, sex, ethnicity, myocardial infarction history, diabetes, hypertension, and heart rate.*

FDA Label Image

Debossed Symbol (44a4e8de 0430 48f8 8178 093afcded438 03)

Carton label for Metoprolol Succinate extended-release tablets, 25 mg, with 90 tablets per bottle. The label displays the brand name Metoprolol Succinate prominently, indicates the strength as 25 mg, and shows the quantity as 90 tablets. The labeler is Rebel Distributors Corp. The label includes the product NDC: 21695-950-02.*

FDA Label Image

Metoprolol Succinate 50mg (44a4e8de 0430 48f8 8178 093afcded438 04)

Metoprolol Succinate 50 mg extended-release tablets label showing a pack of 30 tablets. The label features Physician Partner branding, lists Watson Laboratories, Inc. as the manufacturer, and provides identifying information including lot number, expiration date, and National Drug Code (NDC) 21695-950-30. The label also includes patient storage instructions and a description of the tablets as white, round, coated, and debossed with a logo.*

* 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.