Ondansetron Hydrochloride Tablet, Film Coated
Product Images NDC 57237-076

3 FDA label images from Rising Pharma Holdings, 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 Hydrochloride (NDC 57237-076). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rising Pharma Holdings, 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.

Product Images & Figures Index

FDA Label Image

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

Package Label-principal Display Panel (4 mg (30 Tablet Bottle))
Label for Ondansetron Tablets USP 4 mg, film-coated tablets, containing 30 tablets. The label includes the NDC 57237-075-30, distributed by Rising Health, LLC, Saddle Brook, NJ, and made in India. It also provides storage instructions and dosage note, marked as Rx only.*
FDA Label Image

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

Package Label-principal Display Panel (8 mg (30 Tablet Bottle))
Ondansetron Hydrochloride 8 mg film-coated tablets packaging label from Rising Pharma Holdings, Inc. The package contains 30 tablets for oral use. The label includes storage instructions, dosage note, and distribution information by Rising Health, LLC in Saddle Brook, NJ. The product is made in India and marked as Rx only.*
FDA Label Image

Chemical Structure (Ondansetron Str)

Chemical Structure (Ondansetron Str)
Chemical structure of Ondansetron Hydrochloride dihydrate. The diagram shows the molecular composition including rings, nitrogen atoms, a ketone group, and the associated hydrochloride and two water molecules.*

* 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.