USFDA APPLICATION NUMBER - 20212 / DOSAGE - INJECTABLE;INJECTION - EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
DEXRAZOXANE HYDROCHLORIDE(UNII: 5346058Q7S) (DEXRAZOXANE - UNII:048L81261F) | DEXRAZOXANE | 500mg in 50 | 250mg in 25 |
Inactive Ingredients
Ingredient Name | Pharmacia and Upjohn Company LLC |
---|---|
HYDROCHLORIC ACID(QTT17582CB) |