Palonosetron Injection, Solution
Product Images NDC 63323-673

9 FDA label images from Fresenius Kabi Usa, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Palonosetron (NDC 63323-673). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, Llc, 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 (Pal0b 0001 01)

Structural Formula (Pal0b 0001 01)
Chemical structure of Palonosetron hydrochloride, showing its molecular configuration with a fused ring system and nitrogen atoms, consistent with the active ingredient Palonosetron in the injection solution product by Fresenius Kabi USA, LLC.*
FDA Label Image

Figure (Pal0b 0001 02)

Figure (Pal0b 0001 02)
A vertical bar chart showing differences in complete response rates. The horizontal axis displays values from -10 to 35, while bars represent percentage differences with confidence intervals ranging from approximately -9% to 35%. The chart likely compares treatment response rates but contains no specific drug names or labels visible in the image.*
FDA Label Image

Figure (Pal0b 0001 03)

Figure (Pal0b 0001 03)
A horizontal bar chart illustrating the difference in complete response rates with 95% confidence intervals for a medical treatment. The x-axis represents percentage differences ranging from -10% to 40%, and the data points show positive differences favoring palonosetron.*
FDA Label Image

Figure (Pal0b 0001 04)

Figure (Pal0b 0001 04)
A horizontal bar chart labeled 'Difference in C-peptide Response Rate' with percentage values ranging approximately from -10% to 40%. The chart has two labeled intervals: one between 7% and 31%, and another between 0% and 24%, possibly representing confidence intervals or effect size ranges.*
FDA Label Image

Figure (Pal0b 0001 05)

Figure (Pal0b 0001 05)
Palonosetron 0.25 mg/5 mL injection solution carton for intravenous use. The packaging shows the product name Palonosetron with concentration and route of administration. The labeler is Fresenius Kabi USA, LLC. The design is predominantly white with black text and includes the company logo in a clean, modern font.*
FDA Label Image

Figure (Pal0b 0001 06)

Figure (Pal0b 0001 06)
Palonosetron injection, solution 0.25 mg/5 mL vial from Fresenius Kabi USA, LLC. The label includes the proprietary name Palonosetron, strength, dosage form, and labeler name on a white background with black text.*
FDA Label Image

Package Label (PRINCIPAL DISPLAY PANEL -  Palonosetron Hydrochloride 0.25 mg Single-Dose Prefilled Syringe Label)

Package Label (PRINCIPAL DISPLAY PANEL -  Palonosetron Hydrochloride 0.25 mg Single-Dose Prefilled Syringe Label)
Palonosetron Hydrochloride Injection 0.25 mg per 5 mL (0.05 mg per mL) in a 5 mL single-dose syringe. Label includes NDC 63323-673-21 and is manufactured by Fresenius Kabi USA, LLC. The solution is for intravenous injection only, with instructions to discard unused portions. The label features concentration markings from 1 mL to 5 mL and includes storage and handling information.*
FDA Label Image

Package Label (PRINCIPAL DISPLAY PANEL)

Package Label (PRINCIPAL DISPLAY PANEL)
Palonosetron Hydrochloride Injection 0.25 mg per 5 mL (0.05 mg per mL) single-dose syringe label. The label indicates the product is for intravenous injection only and includes instructions to discard unused portion. The labeler is Fresenius Kabi USA, LLC, with NDC 63323-673.*
FDA Label Image

Package Label (PRINCIPAL DISPLAY PANEL)

Package Label (PRINCIPAL DISPLAY PANEL)
Palonosetron Hydrochloride Injection 0.25 mg per 5 mL (0.05 mg per mL) label for intravenous injection. The packaging indicates single-dose syringes, 10 x 5 mL, labeled by Fresenius Kabi USA, LLC.*

* 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.