Metoclopramide Tablet
Product Images NDC 55154-4383

3 FDA label images from Cardinal Health 107, Llc · 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 Metoclopramide (NDC 55154-4383). 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

Bag Label (B99b1059 6f6a 444d 9ce2 E6a9ce66ff28 00)

Bag Label (B99b1059 6f6a 444d 9ce2 E6a9ce66ff28 00)
Label for Metoclopramide Tablets USP 10 mg, containing 10 tablets. The label includes storage instructions, a warning about packaging not being child resistant, and manufacturing information. It mentions manufacturing in Croatia by Pliva Hrvatska d.o.o. and distribution by Cardinal Health and Mylan Institutional Inc.*
FDA Label Image

Bag Label (B99b1059 6f6a 444d 9ce2 E6a9ce66ff28 01)

Bag Label (B99b1059 6f6a 444d 9ce2 E6a9ce66ff28 01)
Label of Metoclopramide Tablets USP 5 mg showing a package containing 10 tablets. The label includes dosage form as oral tablets, storage instructions at controlled room temperature, and manufacturer details including production in Croatia and distribution by Cardinal Health and Mylan Institutional Inc. It states the package is for institutional use only, not child resistant, and provides warnings to keep out of reach of children.*
FDA Label Image

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Chemical structure of metoclopramide, showing a benzene ring with chlorine, amino, and methoxy groups, with an attached diethylaminoethyl side chain, along with associated hydrochloride and water molecules.*

* 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.