Ondansetron Hydrochloride Tablet, Film Coated
Product Images NDC 68071-4705

2 FDA label images from Nucare Pharmaceuticals,inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ondansetron Hydrochloride (NDC 68071-4705). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare Pharmaceuticals,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

Pdp (68071 4705 04 A176)

Pdp (68071 4705 04 A176)
Ondansetron Hydrochloride 8 mg film-coated tablets label from NuCare Pharmaceuticals, Inc. The label includes the NDC 68071-4705-4, lot number placeholder, and expiration date placeholder. It describes the tablets as oval-shaped yellow tablets debossed with 'F' on one side and '92' on the other. Instructions specify to take the tablets every 4 hours. The label also contains storage instructions and barcodes.*
FDA Label Image

Chemical Structure (Ondansetron Str)

Chemical Structure (Ondansetron Str)
Chemical structure of Ondansetron Hydrochloride, showing the molecular formula with a fused aromatic ring system, a ketone group, a methyl-substituted nitrogen, and a substituted imidazole ring, including 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.