USFDA APPLICATION NUMBER - 208374 / DOSAGE - SOLUTION;INTRAVENOUS - 500MG/100ML (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) |
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