Metoprolol Succinate Tablet, Extended Release
Product Images NDC 63629-9413

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 63629-9413). 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 (118706c2 F03f 4175 Aba2 4f0cddb75ae7 01)

Figure (118706c2 F03f 4175 Aba2 4f0cddb75ae7 01)
Chemical structure of metoprolol succinate depicted as two connected parts: the metoprolol moiety on the left and the succinate moiety on the right, shown with detailed molecular bonds and groups.*
FDA Label Image

Figure (118706c2 F03f 4175 Aba2 4f0cddb75ae7 02)

Figure (118706c2 F03f 4175 Aba2 4f0cddb75ae7 02)
A forest plot chart titled 'Results for Subgroups in MERIT-HF' displaying relative risk and 95% confidence intervals for total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure. It compares outcomes for subgroups receiving metoprolol succinate versus placebo across categories such as geography, NYHA class, ejection fraction, etiology, sex, race, myocardial infarction history, diabetes, hypertension, and heart rate.*
FDA Label Image

Label (Lbl636299413)

Label (Lbl636299413)
Label for metoprolol succinate extended-release 200 mg tablets by Bryant Ranch Prepack, packaging count 30 tablets. The label includes storage instructions at 20-25°C (68-77°F), a warning to keep drugs out of reach of children, and a barcode with NDC 63629-9413. The tablets are described as white to off-white oval, size 5;67.*

* 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.