Empirical Formula (22c9339b Figure 01)
Desmopressin Acetate Tablet
Product Images NDC 10702-169
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 10702-169). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Kvk-tech, 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.
Kvk Logo (22c9339b Figure 02)
0.1 mg Container Lable (22c9339b Figure 03)
Desmopressin Acetate Tablets are a prescription medication containing 0.1mg of Desmopressin Acetate, which is used for treating certain conditions such as diabetes insipidus and bedwetting. The medication comes in a bottle containing 100 tablets, and dosage information is available in the package insert. It should be dispensed in a tightly sealed, child-resistant container and stored between 20°C and 25°C. The manufacturer of this product is KVK-Tech, Inc. based in Newtown, Pennsylvania, and the product is made in the USA. The NDC number for this medication is 10702-169-01.*
0.2 mg Container Lable (22c9339b Figure 04)
Desmopressin Acetate Tablets, with 0.2mg strength and RxOnly prescription, are manufactured by KVK-Tach Inc. and come in a container of 100 tablets. The tablets contain Desmopressin Acstate, USP. 02mg as its active ingredient. The package insert provides necessary dosage information for administration. It is advised to store the tablets in a tightly packed child-resistant container at room temperature (excursions allowed) and avoid exposure to light and heat. The product comprises a warning to keep it out of children's reach. The product label shows NDC 10702-170-01.*
* 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.
