Strength
4 ug/mL
Manufacturer
Sun Pharmaceutical Industries Inc.NDC
62756052940
Classification
Generic
Dosage Form
INJECTION, SOLUTION
Route
INTRAVENOUS; SUBCUTANEOUS
Last Updated
9/17/2025
Active Ingredients
DESMOPRESSIN ACETATEApproval Type
Generic (ANDA)
FDA Application
ANDA091280On Market Since
2/20/2014
Pharmacological Classes
Factor VIII Activator
Increased Coagulation Factor VIII Activity
Increased Coagulation Factor VIII Concentration
Vasopressin Analog
Vasopressins
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