
USFDA APPLICATION NUMBER - 208374 / DOSAGE - SOLUTION;INTRAVENOUS - 250MG/50ML (5MG/ML)
| Active Ingredient/Active Moiety | ||
| Ingredient Name | Basis of Strength | Strength |
|---|---|---|
| BIVALIRUDIN(UNII: TN9BEX005G) (BIVALIRUDIN - UNII:TN9BEX005G) | BIVALIRUDIN | 500mg in 100 | 250mg in 50 |
Inactive Ingredients
| Ingredient Name | Baxter Healthcare Corporation |
|---|---|
| HYDROCHLORIC ACID(QTT17582CB) | |
| SODIUM CHLORIDE(451W47IQ8X) | |
| SODIUM HYDROXIDE(55X04QC32I) | |
| WATER(059QF0KO0R) |