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USFDA APPLICATION NUMBER - 18938 / DOSAGE - INJECTABLE;INJECTION - 0.004MG/ML
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| desmopressin acetate(UNII: XB13HYU18U) (desmopressin - UNII:ENR1LLB0FP) | desmopressin | 4ug in 1 | 4ug in 1 |
Inactive Ingredients
| Ingredient Name | Sun Pharmaceutical Industries, Inc. | American Regent, Inc. | Ferring Pharmaceuticals Inc. | sanofi-aventis U.S. LLC | Teva Parenteral Medicines, Inc. | Hospira, Inc. |
|---|---|---|---|---|---|---|
| CHLOROBUTANOL HEMIHYDRATE(3X4P6271OX) | ||||||
| CHLOROBUTANOL(HM4YQM8WRC) | ||||||
| HYDROCHLORIC ACID(QTT17582CB) | ||||||
| SODIUM CHLORIDE(451W47IQ8X) | ||||||
| WATER(059QF0KO0R) |
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