Ganirelix Acetate Injection, Solution
Product Images NDC 71288-554

3 FDA label images from Meitheal Pharmaceuticals Inc. · 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 71288-554). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meitheal 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.

Product Images & Figures Index

FDA Label Image

Structural Formula (Gan05 0000 01)

Structural Formula (Gan05 0000 01)
Chemical structure diagram showing a portion of the Ganirelix Acetate molecule with labeled amino acid residues and associated chemical groups.*
FDA Label Image

Ganirelix Syringe Label (Gan05 0000 02 V4)

Ganirelix Syringe Label (Gan05 0000 02 V4)
Label for Ganirelix Acetate Injection 250 mcg per 0.5 mL, a subcutaneous single-dose sterile prefilled syringe with a 29 gauge by 1/2 inch needle. The product is manufactured for Meitheal Pharmaceuticals Inc., Chicago, IL, and made in China. The label includes storage instructions to protect from light and advises discarding unused portions. The NDC 71288-554-80 is displayed along with a barcode.*
FDA Label Image

Ganirelix Carton (Gan05 0000 03 V6)

Ganirelix Carton (Gan05 0000 03 V6)
Ganirelix Acetate Injection 250 mcg per 0.5 mL subcutaneous solution in a single-dose sterile prefilled syringe. The carton includes dosage strength and route of administration. Labeler is Meitheal Pharmaceuticals Inc., with NDC 71288-554-80. Packaging specifies a 29 gauge, 1/2 inch needle and indicates Rx only.*

* 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.