Ondansetron Hydrochloride Tablet, Film Coated
Product Images NDC 70518-1585

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ondansetron Hydrochloride (NDC 70518-1585). 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

Ondansetron 4mg 70518 1585 01

Ondansetron 4 mg tablet packaging label indicating 30 tablets per quantity. The label shows the product is repackaged by RemedyRepack Inc. and manufactured by Aurobindo, India. It includes storage instructions and a QR code, with a note to keep medication out of children’s reach. The label states 'RX ONLY' and directs users to see the package insert for usage directions.*

FDA Label Image

Ondansetron 4mg 70518 1585 02

Ondansetron Hydrochloride 4 mg film-coated tablets packaging label showing quantity of 60 tablets. The label includes the proprietary name Ondansetron, strength of 4 mg, dosage form as tablet, and indicates repackaging by RemedyRepack Inc. It also lists manufacturer information for Aurobindo, India, and storage instructions.*

FDA Label Image

Remedy_label (Remedy Label)

Ondansetron Hydrochloride 4 mg film-coated tablets packaging label showing a quantity of 30 tablets. The label includes the NDC 70518-1585-00 and mentions repackaging by RemedyRepack Inc. It also notes manufacturing by Aurobindo, India, with storage instructions and a QR code present.*

* 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.