Logo (Desmopressin 04)
Desmopressin Acetate Solution
Product Images NDC 69918-901
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Desmopressin Acetate (NDC 69918-901). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Nordic Pharma, 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.
Figure 1 (Desmopressin Acetate 01)
Label for Desmopressin Acetate Injection 40 mcg/10 mL (4 mcg/mL) solution in a 10 mL multiple-dose vial. The label states use for intravenous and subcutaneous use only and indicates prescription status. Manufactured for Amring Pharmaceuticals Inc. by a company in Sweden, labeled by Nordic Pharma, Inc.*
Figure 2 (Desmopressin Acetate 02)
Desmopressin Acetate Injection 40 mcg/10 mL (4 mcg/mL) solution for intravenous and subcutaneous use. The label indicates a 10 mL multiple-dose vial and includes storage instructions to refrigerate. Manufactured for Amring Pharmaceuticals Inc. and labeled with the novaplus logo.*
Figure 3 (Desmopressin Acetate 04)
Desmopressin Acetate Injection 4 mcg/mL solution for intravenous and subcutaneous use, preservative free. The label indicates packaging of ten 1 mL single-dose ampules, with instructions for use and storage conditions. Manufactured for Amring Pharmaceuticals, the label also displays the NDC 69918-899-11 and the NovaPlus brand logo.*
Structural Formula (Desmopressin Acetate)
Chemical structure diagram of Desmopressin Acetate showing its peptide chain sequence and molecular components, including amino acid residues and associated chemical groups.*
* 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.
