Ondansetron Injection
Product Images NDC 60505-6130

3 FDA label images from Apotex Corp. · 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 (NDC 60505-6130). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Apotex Corp., 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

Ondansetron Hydrochloride Chemical Structure (Ondansetron 01)

Ondansetron Hydrochloride Chemical Structure (Ondansetron 01)
Chemical structure of ondansetron hydrochloride dihydrate, showing the molecular arrangement of the active ingredient in the product Ondansetron 2 mg/mL injection by Apotex Corp.*
FDA Label Image

Ondansetron Injection Usp Label Image (2 mL Single-use Vials)

Ondansetron Injection Usp Label Image (2 mL Single-use Vials)
ONDANSETRON Injection, USP 4 mg per 2 mL (2 mg/mL) single-dose vial label for intramuscular or intravenous use only. Manufactured by Qilu Pharmaceutical (Hainan) Co., Ltd. for Apotex Corp. The label includes the product NDC 60505-6130 and Apotex Corp. branding.*
FDA Label Image

Ondansetron Injection Usp Label Image (25 x 2 mL Single-use Vials)

Ondansetron Injection Usp Label Image (25 x 2 mL Single-use Vials)
Ondansetron Injection USP 4 mg/2 mL (2 mg/mL) vial carton from Apotex Corp. The label shows this is an intramuscular or intravenous injection, sterile, for prescription use only. The package contains 25x2 mL single-dose vials. Dosage instructions and storage conditions (2° to 30°C, protect from light) are included. The label also lists manufacturing by Qilu Pharmaceutical (China) for Apotex in the USA.*

* 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.