Motegrity Tablet, Film Coated
Product Images NDC 54092-546

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Motegrity (NDC 54092-546). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Takeda Pharmaceuticals America, 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

Chemical Structure (Motegrity 01)

Chemical structure diagram showing the molecular formula of prucalopride, the active ingredient in Motegrity tablets. The structure includes elements such as chlorine, nitrogen, oxygen, and carboxylic acid functional groups.*

FDA Label Image

Principal Display Panel (1 mg Tablet Bottle Label)

Label for MOTEGRITY 1 mg tablets, film-coated oral tablets containing prucalopride. The label states storage instructions, usual dosage of one tablet daily, and packaging of 30 tablets. Distributed by Takeda Pharmaceuticals America, Inc., Lexington, MA. Includes barcode and trademark information.*

FDA Label Image

Principal Display Panel (2 mg Tablet Bottle Carton)

MOTEGRITY 2 mg tablets packaging label for oral use contains prucalopride as the active ingredient. The label includes storage instructions, dosage information stating 'one tablet once daily,' and notes that it is a patient sample not for sale. The package contains 30 film-coated tablets and is labeled by Takeda Pharmaceuticals America, Inc. The label bears the NDC 54092-547-03 and includes Takeda logos and trademark information.*

* 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.