Prucalopride Tablet, Film Coated
Product Images NDC 0054-0749

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Prucalopride (NDC 0054-0749). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa Inc, 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

Prucalopride-structural-formula-image (Image 01)

Chemical structure diagram of prucalopride, showing its molecular components including a chlorinated aromatic ring and attached nitrogenous groups.*

FDA Label Image

Prucalopride 1 mg Bottle Label (Image 02)

Label for Prucalopride Tablets 1 mg, a human prescription oral film-coated tablet. The label states the package contains 30 tablets, distributed by Hikma Pharmaceuticals USA Inc. It includes storage instructions and the NDC number 0054-0749-13. The label features the Hikma logo and dosage information.*

FDA Label Image

Prucalopride 2 mg Bottle Label (Image 03)

Label for Prucalopride 2 mg tablets, film coated, oral use. The label indicates 30 tablets per package, with NDC 0054-0750-13. Distributed by Hikma Pharmaceuticals USA Inc., Berkeley Heights, NJ. The label includes storage instructions and dosage information, noting one tablet once daily.*

* 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.