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/ DOSAGE - SPRAY, METERED;NASAL - 0.01MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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) |
LOOKING FOR A SUPPLIER?