Ondansetron Tablet, Orally Disintegrating
Product Images NDC 70518-1551

3 FDA label images from Remedyrepack Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ondansetron (NDC 70518-1551). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Mm2 (Ondansetron 8mg 70518 1551 01)

Mm2 (Ondansetron 8mg 70518 1551 01)
Ondansetron 8 mg orally disintegrating tablets packaging label showing quantity of 30 tablets. Label includes the National Drug Code (NDC) 70518-1551-01, manufacturing source Aurobindo Pharma, Hyderabad, India, and repackaging information by RemedyRepack Inc. Directions for use refer to the package insert. The label also contains storage instructions and a QR code.*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Ondansetron 8 mg orally disintegrating tablets packaging label showing a quantity of 6 tablets. The label includes the NDC number 70518-1551-00, manufacturer information (Aurobindo Pharma, Hyderabad, India), and repackaging details by RemedyRepack Inc. The label highlights the oral disintegrating dosage form and dosage strength.*
FDA Label Image

Chemical Structure (Ondansetronod Str)

Chemical Structure (Ondansetronod Str)
Chemical structure diagram of ondansetron, illustrating its molecular framework including fused rings and side chains, as relevant to the active pharmaceutical ingredient ondansetron.*

* 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.