Desmopressin Acetate 72843-0459
Product NDC
72843-0459- Manufacturer
- Ubi Pharma Inc.
- Dosage Form
- Injection
- Route
- Intravenous And Subcutaneous
- Product Type
- Human Prescription Drug
- Marketing Start
- February 14, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA210218
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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]
Packaging Options(1)
10 AMPULE in 1 BOX (72843-459-10) / 1 mL in 1 AMPULE