Deferiprone Tablet, Coated
Product Images NDC 0054-0711

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Deferiprone (NDC 0054-0711). 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

Deferiprone-chem-structure.jpg (Deferiprone Chem Structure)

Chemical structure of deferiprone showing a six-membered aromatic ring with hydroxyl, carbonyl, methyl, and methylated nitrogen functional groups.*

FDA Label Image

Deferiprone-tabs-1000mg-50s-bottle-label (Image 03)

Label for Deferiprone tablets, 1000 mg strength, in a 50-tablet bottle. The label includes the NDC 0054-0711-19 and indicates a dosage instruction "three-times-a-day." Distributed by Hikma Pharmaceuticals USA Inc., Berkeley Heights, NJ. The label advises storage at 20° to 25°C and notes this is prescription only (Rx only).*

FDA Label Image

Deferiprone-tabs-1000mg-150s-bottle-label (Image 04)

Deferiprone 1000 mg coated tablets label from Hikma Pharmaceuticals USA Inc. The label specifies oral dosage strength and directs pharmacists to dispense an accompanying Medication Guide. Storage instructions, usual dosage timing (three-times-a-day), and packaging details for 150 tablets are shown, including a barcode and the NDC 0054-0711-23.*

FDA Label Image

Deferiprone-tabs-1000mg-300s-bottle-label (Image 05)

Label for Deferiprone Tablets, 1000 mg, oral coated tablets, supplied in a 300 tablet package. The label highlights dosing as three times a day, includes storage instructions at controlled room temperature, and notes distribution by Hikma Pharmaceuticals USA Inc.*

* 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.