Ondansetron Tablet
Product Images NDC 69339-172

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Ondansetron (NDC 69339-172). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Natco Pharma Usa Llc, 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

4mg-30 Label (Ondansetron 4mg 30s)

This is a prescription medication with the National Drug Code 69339-171-03. Each film-coated tablet contains 5mg of ondansetron hydrochloride dihydrate, equivalent to 4 mg of ondansetron. The tablets are controlled for dissolution, and it is intended only for use as directed by medical personnel. The package insert should be consulted for dosage and administration recommendations. The product is stored between 20°-25°C (68°-77°F) and meets the USP dissolution test 3. The manufacturer is Natco Pharma Limited, India, and the product is distributed by DASH Pharmaceuticals LLC in Upper Saddle River, NJ, USA.*

FDA Label Image

4mg-500 Label (Ondansetron 4mg 500s)

This is a medication called Ondansetron, containing 5mg of ondansetron hydrochloride dihydrate which is equivalent to 4mg of ondansetron. It comes in a film-coated tablet form and should be administered as directed based on the package insert. It meets USP Dissolution Test 3 and should be stored in a tight, light-resistant container at a controlled room temperature of 20°- 25°C (68°-77°F). It comes in a package of 500 tablets and is manufactured by Natco Pharma Limited in India for DASH Pharmaceuticals LLC based in Upper Saddle River, NJ, USA. The GTIN code is 00369339171059.*

FDA Label Image

8mg-30 Label (Ondansetron 8mg 30s)

This is a description of a medication called Ondansetron Hydrochloride Dihydrate. It comes in film-coated tablets, with each tablet containing 10mg of the medication. The tablets are dispensed in a tight, light-resistant container as defined by the USP. The medication meets USP Dissolution Test 3. The package insert should be consulted for dosage and administration instructions. The medication is manufactured by Natco Pharma Limited in India and distributed in the US by DASH Pharmaceuticals LLC.*

FDA Label Image

8mg-500 Label (Ondansetron 8mg 500s)

Each film-coated tablet of ondansetron hydrochloride dihydrate contains 10 mg of the active ingredient. The equivalent of 8 mg of ondansetron is available in each tablet. The package insert provides instructions for dosing and administration. The tablets should be stored in a tight, light-resistant container at controlled room temperature. This product meets the USP Dissolution Test 3. The tablets are available in a package of 500 and are available by prescription only. This medication is manufactured by Natco Pharma Limited, India, and distributed by DASH Pharmaceuticals LLC, Upper Saddle River, NJ.*

FDA Label Image

Structure (Structure)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.