Ondansetron Injection
Product Images NDC 72572-520

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ondansetron (NDC 72572-520). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Civica, 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

Structural Formula (Ondansetron Injection Civica 1)

FDA Label Image

462-816-00 (Ondansetron Injection Civica 2)

462-816-00 (Ondansetron Injection   Civica 2)
This is a description of Ondansetron Injection, which is used for intravenous or intramuscular injection. The medication comes in a 2 mL single-dose vial and needs to be protected from light. The manufacturer is Civica, Inc. and it is a prescription-only drug. The remaining characters are Lot and Expiration date numbers.*
FDA Label Image

462-817-00 (Ondansetron Injection Civica 3)

462-817-00 (Ondansetron Injection   Civica 3)
This is a description of a medication called Ondansetron injection. The solution comes in a 1mL single-dose vial containing 2mg ondansetron as ondansetron hydrochloride dihydrate, sodium chloride, sodium citrate dihydrate, and buffer. The package insert should be consulted for dosage and administration. The vials should be stored at a controlled room temperature of 20° to 25°C and protected from light.*
FDA Label Image

Layout 1 (Ondansetron Injection Civica 4)

Layout 1 (Ondansetron Injection   Civica 4)
This text contains product identification and expiration information such as the Global Trade Item Number (GTIN), serial number (SN), expiration date ("EXP"), and lot number (LOT). However, there is no specific product or context provided for these codes.*

* 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.