
USFDA APPLICATION NUMBER - 17922 / DOSAGE - SOLUTION;NASAL - 0.01%
| 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) |
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