Motofen Tablet
Product Images NDC 54766-200

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Motofen (NDC 54766-200). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sebela Pharmaceuticals 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

Ca20010001 Motofen

Packaging label for Motofen tablets, containing difenoxin and atropine sulfate. Each tablet has a strength of 1 mg/0.025 mg. The label shows a 100 tablet bottle distributed by Sebela Pharmaceuticals Inc., with the product NDC 54766-200-10. The label features dosage information, storage instructions, and a barcode.*

FDA Label Image

100 Count Bottle Label (Picture1)

Motofen 1 mg / 0.025 mg tablets containing difenoxin and atropine sulfate, labeled for oral use. The label shows the product name, active ingredients, strengths, package size of 100 tablets, the labeler Sebela Pharmaceuticals Inc., and storage instructions. It also includes dosage information and a barcode with NDC 54766-200-10.*

FDA Label Image

Difenoxin Hydrochloride (Motofen 01)

Chemical structure of difenoxin hydrochloride, the active ingredient in Motofen tablets (difenoxin and atropine sulfate). The structure includes phenyl groups, a piperidine ring, and nitrile substitution, with a hydrochloride component indicated.*

FDA Label Image

Atropine Sulfate (Motofen 02)

Chemical structure of atropine sulfate, showing the molecular arrangement of atoms including a tropane ring and sulfate groups, labeled as atropine sulfate in the image.*

* 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.