Rolvedon Injection, Solution
Product Images NDC 76961-101

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Rolvedon (NDC 76961-101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Spectrum Pharmaceuticals, 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

Duration Of Severe Neutropenia (dsn) Graphs (Image 01)

Two bar charts presenting the duration in days of severe neutropenia during Cycle 1 from two studies, comparing Rolvedon and Pegfilgrastim. Study 1 (n=406) shows patient percentages across no severe neutropenia, 1 to 3 days, and ≥4 days. Study 2 (n=237) displays similar data up to 3 days and ≥4 days, with percentages indicated for each category.*

FDA Label Image

Syringe Label (Image 02)

Rolvedon (eflapegrastim-xnst) injection label showing strength 13.2 mg/0.6 mL. The label indicates manufacture by Spectrum Pharmaceuticals, Inc. It includes a barcode and numeric code supporting product identification.*

FDA Label Image

Blister Tray Label (Image 03)

Label of Rolvedon (eflapegrastim-xnst) injection 13.2 mg/0.6 mL, a sterile, preservative-free solution for subcutaneous injection in a single-dose pre-filled 0.6 mL syringe. The label includes storage instructions (36°F to 46°F, protect from light, do not freeze or shake), manufacturer Spectrum Pharmaceuticals, Inc., and NDC 76961-101-01.*

FDA Label Image

Carton Labeling (Image 04)

Rolvedon 13.2 mg/0.6 mL (eflapegrastim-xnst) injection carton label for subcutaneous use. The label features the brand and generic names, dosage strength, administration route, and usage instructions. The labeler is Spectrum Pharmaceuticals, Inc., with storage instructions and a barcode visible.*

* 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.