Desmopressin Acetate Injection, Solution
Product Images NDC 65219-293

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Desmopressin Acetate (NDC 65219-293). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, 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.

FDA Label Image

Desmopressin-acetate (Des0e 0000 01)

Desmopressin-acetate (Des0e 0000 01)
Chemical structure of Desmopressin Acetate, showing its peptide sequence with amino acid residues and associated molecular groups as depicted in the image.*
FDA Label Image

Fresenius Kabi Logo (Des0e 0000 02)

FDA Label Image

Package Label – Principal Display Panel – 4 Mcg – Shelf Carton (Des0e 0000 03)

Package Label – Principal Display Panel – 4 Mcg – Shelf Carton (Des0e 0000 03)
Packaging label for Desmopressin Acetate Injection, USP 4 mcg/mL preservative-free solution for intravenous and subcutaneous use. The label indicates 10 x 1 mL single-dose vials. Manufactured for Fresenius Kabi USA, LLC. Storage instructions include refrigeration at 2°-8°C (36°-46°F).*
FDA Label Image

Package Label – Principal Display Panel – 4 Mcg – Vial Label (Des0e 0000 04)

Package Label – Principal Display Panel – 4 Mcg – Vial Label (Des0e 0000 04)
Label of Desmopressin Acetate Injection, USP 4 mcg/mL preservative-free solution in a 1 mL single-dose vial. It is intended for intravenous and subcutaneous use only. The label includes storage instructions to refrigerate between 2° to 8°C (36° to 46°F) and disposal guidance for unused portions. Manufactured for Fresenius Kabi USA, LLC, Lake Zurich, IL.*

* 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.