Ondansetron Hydrochloride Tablet, Film Coated
Product Images NDC 67296-1562

View Photos of 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 Hydrochloride (NDC 67296-1562). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Package Label-principal Display Panel (4 mg (30 Tablet Bottle))

Package Label-principal Display Panel (4 mg (30 Tablet Bottle))
Ondansetron Tablets, USP 4 mg film-coated tablets label by Rising Pharmaceuticals, indicating 30 tablets per package. The label includes NDC 57237-075-30, storage instructions, and notes that the product is distributed by Rising Pharma Holdings, Inc., East Brunswick, NJ, and made in India. It also highlights prescription-only status and space for coding and serialization.*
FDA Label Image

Package Label-principal Display Panel (8 mg (30 Tablet Bottle))

Package Label-principal Display Panel (8 mg (30 Tablet Bottle))
Ondansetron Tablets USP 8 mg label for a 30-tablet pack by RedPharm Drug, Inc. The label states each film-coated tablet contains ondansetron hydrochloride USP dihydrate equivalent to 8 mg of ondansetron. It includes storage instructions, distributor information, a barcode, and notes on packaging and coding areas. The product is Rx only and made in India.*
FDA Label Image

Chemical Structure (Ondansetron Str)

Chemical Structure (Ondansetron Str)
Chemical structure of Ondansetron Hydrochloride Dihydrate, depicting the molecular arrangement with ketone, indole, and imidazole rings, along with the hydrochloride and two water molecules of hydration.*

* 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.