Ganirelix Acetate Injection, Solution
Product Images NDC 68083-472

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 68083-472). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gland Pharma Limited, 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

Ganirelix-spl-carton-label (Ganirelix Spl Carton Label)

Ganirelix-spl-carton-label (Ganirelix Spl Carton Label)
Ganirelix Acetate Injection 250 mcg/0.5 mL single-dose sterile prefilled syringe carton. The label specifies subcutaneous use, includes the NDC 68083-472-01, and mentions a 27 gauge by 1/2 inch needle. Manufactured by Gland Pharma Limited, with storage and composition details noted. Packaging is free from latex components.*
FDA Label Image

Ganirelix-spl-structure (Ganirelix Spl Structure)

Ganirelix-spl-structure (Ganirelix Spl Structure)
Chemical structure diagram of Ganirelix Acetate showing the molecular arrangement of its peptide chain with labeled amino acid residues and chemical groups. The structure includes annotations for specific amino acids and side chains characteristic of Ganirelix Acetate.*
FDA Label Image

Ganirelix-spl-vial-label (Ganirelix Spl Vial Label)

Ganirelix-spl-vial-label (Ganirelix Spl Vial Label)
Label for Ganirelix Acetate Injection 250 mcg/0.5 mL in a single-dose sterile prefilled syringe with a 27 gauge by 1/2 inch needle. The label indicates subcutaneous use, includes storage instructions to protect from light and discard unused portion. Manufactured by Gland Pharma Limited, India. Includes NDC 68083-472-01 and a barcode.*

* 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.