Desmopressin Acetate Injection, Solution
Product Images NDC 62756-529

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Desmopressin Acetate (NDC 62756-529). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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.

FDA Label Image

Carton (Spl Carton)

Desmopressin Acetate Injection is a medication used for intravenous/subcutaneous use only. Each mL of the injection contains 4 mcg desmopressin acetate, USP, 5 mg of chlorobutanol, 9 mg sodium chloride, hydrochloric acid to adjust pH to 4, and water for injection q.s. to 1 mL. It is kept refrigerated at 2° to 8°C (36° to 46°F) and must be preserved in tight containers, protected from light. The package insert must be consulted for dosage information. The medication should be kept out of reach of children. It is distributed by Sun Pharmaceutical Industries, Inc. and manufactured by Sun Pharmaceutical Industries Ltd.*

FDA Label Image

Chem (Spl Chemical Str)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.