Ondansetron Injection
Product Images NDC 72572-520

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)

Chemical structure of ondansetron with a hydrochloride dihydrate component, representing the active ingredient in the Ondansetron 2 mg/mL injection product by Civica, Inc.*

FDA Label Image

462-816-00 (Ondansetron Injection Civica 2)

Ondansetron Injection USP label for a 2 mL single dose vial containing 4 mg/2 mL (2 mg/mL) strength. Indicated for intravenous (IV) or intramuscular (IM) injection. Manufactured by Civica, Inc., the label advises protection from light. Includes lot and expiration date fields, barcode, and notes Rx Only.*

FDA Label Image

462-817-00 (Ondansetron Injection Civica 3)

Ondansetron Injection USP 4 mg/2 mL (2 mg/mL) sterile injection label for intravenous or intramuscular use. The label indicates a package containing 25 single-dose vials of 2 mL each. It states the active ingredient ondansetron hydrochloride dihydrate and other components along with storage instructions. The labeler is Civica, Inc., with the product NDC 72572-520.*

FDA Label Image

Layout 1 (Ondansetron Injection Civica 4)

The packaging label for Ondansetron injection, 2 mg/mL, from Civica, Inc. It includes a barcode, GTIN, serial number, expiration date, and lot number placeholders. The label supports intramuscular and intravenous administration routes.*

* 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.