Ganirelix Acetate Injection, Solution
Product Images NDC 70748-274

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ganirelix Acetate (NDC 70748-274). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin 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

Image (C0fdd470 A16f 41c4 9bfa 4240b6ff67e7 01)

Chemical structure of Ganirelix Acetate depicted as a detailed molecular diagram showing atoms and bonds, including functional groups and side chains characteristic of this active pharmaceutical ingredient.*

FDA Label Image

Image (6b562339 0c67 41b1 81ef 5a4e89721353 51 1)

The image shows the label of Ganirelix Acetate injection, solution for subcutaneous use, with a strength of 250 micrograms per 0.5 mL. The packaging indicates it is manufactured by Lupin Pharmaceuticals, Inc. The label displays dosage information and usage instructions for the injection form.*

FDA Label Image

Container Label (C0fdd470 A16f 41c4 9bfa 4240b6ff67e7 02)

Label for Ganirelix Acetate Injection 250 mcg/0.5 mL, a subcutaneous injection in sterile prefilled syringe form. The label includes the NDC 70748-274-01, manufacturer Lupin Pharmaceuticals, Inc., and mentions the syringe needle size 27 ga x 1/2 inch. It also includes storage instructions and a barcode.*

FDA Label Image

Carton Label (C0fdd470 A16f 41c4 9bfa 4240b6ff67e7 03)

Packaging label for Ganirelix Acetate Injection 250 mcg/0.5 mL, a subcutaneous injection solution by Lupin Pharmaceuticals, Inc. The label indicates a single-dose sterile prefilled syringe with a 27 gauge by 1/2 inch needle. Storage instructions and manufacturing details are also 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.