Desmopressin Acetate 70095-0026
Product NDC
70095-0026- Manufacturer
- Sun Pharmaceutical Industries Limited
- Dosage Form
- Injection, Solution
- Route
- Intravenous And Subcutaneous
- Product Type
- Human Prescription Drug
- Marketing Start
- April 3, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA216922
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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 VIAL, SINGLE-DOSE in 1 CARTON (70095-026-02) / 1 mL in 1 VIAL, SINGLE-DOSE (70095-026-01)