Palonosetron Hydrochloride Injection, Solution
Product Images NDC 0781-3312

5 FDA label images from Sandoz Inc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Palonosetron Hydrochloride (NDC 0781-3312). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sandoz 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

Palonosetron 01

Palonosetron 01
Chemical structure diagram of Palonosetron Hydrochloride, showing its molecular framework including rings, nitrogen atoms, and hydrochloride component.*
FDA Label Image

Palonosetron 02

Palonosetron 02
A bar chart illustrating differences in complete response rates with percentage ranges shown on horizontal bars. The x-axis represents the difference in response rates, spanning from -10 to 35 percent. Three horizontal bars display varying ranges from approximately -9% to 23%, indicating comparative data results.*
FDA Label Image

Palonosetron 03

Palonosetron 03
A bar graph showing differences in complete response rates with two data points labeled as [9%, 30%] and [3%, 27%]. The x-axis measures the difference in complete response rates, ranging from -10 to 35%. This likely represents comparative efficacy data.*
FDA Label Image

Palonosetron 04

Palonosetron 04
A bar graph depicting the difference in complete response rates. The x-axis shows values ranging from -10 to 35, and two sets of bars are labeled with percentages: 7% and 31%, and 0% and 24%. The graph compares these percentage differences, but specific categories or treatments are not visible.*
FDA Label Image

Palonosetron 05

Palonosetron 05
Packaging label for Palonosetron HCl Injection 0.25 mg/5 mL (0.05 mg/mL) sterile solution in a 5 mL single-dose vial by Sandoz Inc. The label includes product name, strength, dosage form, route (intravenous), storage instructions, and regulatory information including NDC 0781-3312-75. The label also notes it is for intravenous injection only and is a prescription drug.*

* 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.