Metoprolol Tartrate Tablet, Film Coated
Product Images NDC 55154-4790

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Metoprolol Tartrate (NDC 55154-4790). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cardinal Health 107, 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.

FDA Label Image

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Label for Metoprolol Tartrate Tablets USP 100 mg, film-coated oral tablets in a package of 10. The label includes dosage storage instructions, warnings, and distribution information by Cardinal Health 107, LLC and American Health Packaging.*

FDA Label Image

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Metoprolol Tartrate 50 mg film-coated tablets package label showing 10 tablets. The label displays the active ingredient Metoprolol tartrate USP 50 mg per tablet, storage instructions, warnings about child resistance and protection, and distributor information for Cardinal Health 107, LLC and American Health Packaging.*

FDA Label Image

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Metoprolol Tartrate Tablets USP 25 mg film-coated tablet package label. The label indicates a 10-tablet unit dose container. It includes storage instructions, dosage note to see the full prescribing information, and warnings that the package is not child resistant and is for institutional use only. Labeler and distributor information for Cardinal Health and American Health Packaging is provided along with lot and NDC numbers.*

FDA Label Image

Metoprolol Str

Chemical structure of Metoprolol Tartrate, depicting its molecular arrangement including the tartrate moiety on the right side of the structure.*

* 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.