USFDA APPLICATION NUMBER - 21759 / DOSAGE - INJECTABLE;INTRAVENOUS - 200MG/40ML (5MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Active Ingredient/Active Moiety | ||
Ingredient Name | Basis of Strength | Strength |
---|---|---|
oxaliplatin(UNII: 04ZR38536J) (oxaliplatin - UNII:04ZR38536J) | oxaliplatin | 5mg in 1 | 5mg in 1 |
Inactive Ingredients
Ingredient Name | Aventis Pharma Ltd. | sanofi-aventis U.S. LLC |
---|---|---|
water(059QF0KO0R) |
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