Ganirelix Acetate Injection, Solution
Product Images NDC 67184-0574

View Photos of 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 Ganirelix Acetate (NDC 67184-0574). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Qilu Pharmaceutical Co., Ltd., 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

Image Of Ganirelix Acetate Chemical Structure (Ganirelix 01)

Image Of Ganirelix Acetate Chemical Structure (Ganirelix 01)
Chemical structure diagram depicting the molecular composition and bonds of Ganirelix Acetate, highlighting its complex peptide framework with annotated chemical groups and side chains.*
FDA Label Image

Principal Display Panel (250 mcg/0.5 mL Syringe label)

Principal Display Panel (250 mcg/0.5 mL Syringe label)
Ganirelix Acetate Injection 250 mcg/0.5 mL single-dose sterile prefilled syringe label. The injection is for subcutaneous use with a 27 gauge by 1/2 inch needle. Manufactured by Qilu Pharmaceutical Co., Ltd., Jinan, China. Label includes instructions to discard unused portion and protect from light. Contains a barcode and product NDC 67184-0574.*
FDA Label Image

Principal Display Panel (250 mcg/0.5 mL Carton label)

Principal Display Panel (250 mcg/0.5 mL Carton label)
Ganirelix Acetate Injection 250 mcg/0.5 mL single-dose sterile prefilled syringe carton. The label states the product is for subcutaneous use, free from natural rubber/latex, and manufactured by Qilu Pharmaceutical Co., Ltd., China. It includes a barcode and cautions about storage and handling conditions.*

* 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.