Ondansetron Injection
Product Images NDC 0641-6286

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ondansetron (NDC 0641-6286). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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 Usp Novaplus 1)

Chemical structure of Ondansetron hydrochloride dihydrate, showing its molecular components and arrangement as related to the active ingredient Ondansetron.*

FDA Label Image

Ondansetron Injection, Usp 4 mg/2 mL (2 mg/ml) 2 mL Single Dose Vial (Ondansetron Injection Usp Novaplus 2)

Ondansetron Injection, USP 4 mg per 2 mL (2 mg/mL) vial label from Hikma Pharmaceuticals USA Inc. The label indicates intramuscular (IM) or intravenous (IV) use for this single-dose 2 mL vial. It includes storage instructions to protect from light and displays barcodes, lot number, and expiration date fields.*

FDA Label Image

Ondansetron Injection, Usp 4 mg/2 mL (2 mg/ml) 25 X 2 mL Single Dose Vials (Ondansetron Injection Usp Novaplus 3)

Ondansetron Injection, USP 4 mg per 2 mL (2 mg/mL) single-dose vials. This label displays a 25-count package for intravenous or intramuscular injection. The label indicates the product is sterile, light sensitive, and to be stored at controlled room temperature. Manufactured by Hikma Pharmaceuticals USA Inc.*

FDA Label Image

Ondansetron Injection Usp Novaplus 4

This image shows a label for Ondansetron injection, strength 2 mg/mL, by Hikma Pharmaceuticals USA Inc. The label includes a QR code, a GTIN barcode number, a serial number, an expiration date formatted as MMYYYY, and a lot number.*

* 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.