USFDA APPLICATION NUMBER - 200199 / DOSAGE - SOLUTION;INTRAVENOUS - EQ 3MG BASE/3ML (EQ 1MG BASE/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
TOPOTECAN HYDROCHLORIDE(UNII: 956S425ZCY) (TOPOTECAN - UNII:7M7YKX2N15) | TOPOTECAN HYDROCHLORIDE | 1mg in 1 |
Inactive Ingredients
Ingredient Name | Sandoz Inc |
---|---|
HYDROCHLORIC ACID(QTT17582CB) | |
SODIUM HYDROXIDE(55X04QC32I) | |
TARTARIC ACID(W4888I119H) | |
WATER(059QF0KO0R) |
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