 
				 
										
USFDA APPLICATION NUMBER - 17922 / DOSAGE - SPRAY, METERED;NASAL - 0.01MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength | 
|---|---|---|
| desmopressin acetate(UNII: XB13HYU18U) (desmopressin - UNII:ENR1LLB0FP) | desmopressin | 0.1mg in 1 | 
Inactive Ingredients
| Ingredient Name | Amring Pharmaceuticals, Inc. | Ferring Pharmaceuticals Inc. | sanofi-aventis U.S. LLC | 
|---|---|---|---|
| Benzalkonium Chloride(F5UM2KM3W7) | |||
| chlorobutanol(HM4YQM8WRC) | |||
| citric acid monohydrate(2968PHW8QP) | |||
| Hydrochloric acid(QTT17582CB) | |||
| sodium chloride(451W47IQ8X) | |||
| Sodium Phosphate, Dibasic, Dihydrate(94255I6E2T) |