Leuprolide Acetate Kit
Product Images NDC 72664-611
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 15 technical images submitted to the FDA as part of the official labeling for Leuprolide Acetate (NDC 72664-611). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Vgyaan Pharmaceuticals Llc, 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
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Carton (Vial Carton)
Leuprolide Acetate Injection is a prescription drug with a strength of 4mg/2.8mL. The medicine is for subcutaneous injection containing 1mg of leuprolide acetate in 0.2mL solution. The solution is sterile and contains sodium chloride to adjust tonicity, benzy| alcohol as a preservative and water for injection. The pH range of the solution is 4.0t06.0, and it may contain sodium hydroxide and/or acetic acid. The medication is stored below 77°F (26°C) and must not be frozen or exposed to light. The package insert has complete prescribing information and patient use instructions. Keep out of the reach of children. It is distributed by VGYAAN Pharmaceuticals LLC, Skillman, NJ, and made in the USA.*
Label (Vial Label)
This is a pharmaceutical product labeled as NDC 72664-611-28 containing leupro' ide acetate with a usual dosage of 0.2 mL. It is recommended for subcutaneous injection once daily and should be stored below 77°F (25°C). It is important to protect the product from light and keep it out of the reach of children. The product is distributed by VGYAAN and made in the USA. The package insert should be consulted for more information.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.