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USFDA APPLICATION NUMBER - 21333 / DOSAGE - SPRAY, METERED;NASAL - 0.01MG/SPRAY
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| DESMOPRESSIN ACETATE(UNII: XB13HYU18U) (DESMOPRESSIN - UNII:ENR1LLB0FP) | DESMOPRESSIN ACETATE | 10ug in 0.1 |
Inactive Ingredients
| Ingredient Name | Amring Pharmaceuticals, Inc. | Ferring Pharmaceuticals Inc. | Prasco Laboratories | sanofi-aventis U.S. LLC | Sun Pharmaceutical Industries, Inc. | Bauch & Lomb Incorporated |
|---|---|---|---|---|---|---|
| Benzalkonium chloride(F5UM2KM3W7) | ||||||
| CHLOROBUTANOL(HM4YQM8WRC) | ||||||
| CITRIC ACID MONOHYDRATE(2968PHW8QP) | ||||||
| HYDROCHLORIC ACID(QTT17582CB) | ||||||
| SODIUM CHLORIDE(451W47IQ8X) | ||||||
| SODIUM PHOSPHATE, DIBASIC, DIHYDRATE(94255I6E2T) | ||||||
| WATER(059QF0KO0R) |
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