Desmopressin Acetate 70095-0031-01

Package NDC

70095-0031-01

Manufacturer: Sun Pharmaceutical Industries Limited
Dosage Form: Injection, Solution
Route: Intravenous And Subcutaneous
Product Type: Human Prescription Drug
Marketing Start: June 20, 2023
Listing Expires: December 31, 2026
Application: ANDA216904

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Active Ingredients

Ingredient	Strength
Desmopressin Acetate	4 ug/mL

Drug Class

Factor VIII Activator [EPC]Increased Coagulation Factor VIII Activity [PE]Increased Coagulation Factor VIII Concentration [PE]

Selected Package

70095-0031-01Selected

1 VIAL in 1 CARTON (70095-031-01) / 10 mL in 1 VIAL