Ondansetron Hydrochloride Tablet, Film Coated
Product Images NDC 50268-622

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ondansetron Hydrochloride (NDC 50268-622). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avpak, 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

Label 1 (Screen Shot 2016 08 05 At 3.15.15 Pm)

Ondansetron Hydrochloride 4 mg film-coated oral tablets by AvPAK. The label states 50 tablets (5 x 10 unit doses) with NDC 50268-621-15. It includes dosage form and strength, barcode, storage instructions, and manufacturer details. The label indicates 'Rx Only' and highlights keeping the product out of children's reach.*

FDA Label Image

Label 2 (Screen Shot 2016 08 05 At 3.40.23 Pm)

Packaging label for Ondansetron Hydrochloride Tablets, USP, 8 mg oral film-coated tablets. The label indicates a package of 50 tablets (5 x 10 unit dose) from AvPAK, including NDC 50268-622-15, with storage and handling instructions and manufacturer details.*

FDA Label Image

Chemical Structure (Ondansetron Str)

Chemical structure of Ondansetron Hydrochloride, showing a fused ring system with a ketone group, a methylated nitrogen, and a substituted imidazole ring with associated hydrochloride and dihydrate components.*

* 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.