Deferasirox Tablet, For Suspension
Product Images NDC 67877-550

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Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Deferasirox (NDC 67877-550). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ascend Laboratories, 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

Def 125mg 30tab

Def 125mg 30tab
Label for Deferasirox Tablets for Oral Suspension, 125 mg per tablet. The label indicates a package of 30 tablets, distributed by Ascend Laboratories, LLC, Parsippany, NJ. It includes dosage instructions, storage conditions, and manufacturer information from Alkem Laboratories Ltd., India. The label features a barcode and regulatory notices.*
FDA Label Image

Def 250mg 30tab

Def 250mg 30tab
Label for Deferasirox Tablets for Oral Suspension 250 mg per tablet, oral dosage form. The label states dispensing instructions, storage conditions, manufacturer Alkem Laboratories Ltd., India, and distributor Ascend Laboratories, LLC, Parsippany, NJ. It includes warnings not to chew or swallow whole tablets and indicates a 30-tablet package.*
FDA Label Image

Def 500mg 30tab

Def 500mg 30tab
Label for Deferasirox Tablets for Oral Suspension, 500 mg per tablet, in a 30-tablet bottle. The label instructs that tablets must be dispersed in water or juice before ingestion and includes storage conditions. Manufactured by Alkem Laboratories Ltd., India, and distributed by Ascend Laboratories, LLC.*
FDA Label Image

Def Str

Def Str
Chemical structure diagram of Deferasirox showing its molecular framework with multiple aromatic rings and hydroxyl groups.*

* 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.