Desmopressin Acetate Injection, Solution
Product Images NDC 68083-550

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 Desmopressin Acetate (NDC 68083-550). 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

Desmopressin-acetate (Desmopressin Acetate Empirical Formula)

Desmopressin-acetate (Desmopressin Acetate Empirical Formula)
Chemical structure diagram of Desmopressin Acetate showing its amino acid sequence and chemical groups including sulfhydryl, carboxyl, amide, methyl, and hydrate groups.*
FDA Label Image

Desmopressin-acetate-injection-carton-label (Desmopressin Acetate Injection Carton Label)

Desmopressin-acetate-injection-carton-label (Desmopressin Acetate Injection Carton Label)
Packaging label for Desmopressin Acetate Injection, USP 4 mcg/mL, preservative free, for intravenous and subcutaneous use. The package contains 10 single-dose vials of 1 mL each. Manufactured by Gland Pharma Limited, the label includes storage instructions to keep refrigerated at 2°-8°C (36°-46°F) and dosage administration guidance to see the package insert.*
FDA Label Image

Desmopressin-acetate-injection-container-label (Desmopressin Acetate Injection Container Label)

Desmopressin-acetate-injection-container-label (Desmopressin Acetate Injection Container Label)
Label for Desmopressin Acetate Injection, USP, 4 mcg/mL, preservative-free solution for intravenous and subcutaneous use. The label indicates a 1 mL single-dose vial, manufacturer Gland Pharma Limited, Hyderabad, India, and includes storage instructions to refrigerate at 2°-8°C (36°-46°F). The label also displays the NDC 68083-550-01 and cautions to discard unused portion.*

* 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.