USFDA APPLICATION NUMBER - 20449 / DOSAGE - INJECTABLE;INJECTION - 40MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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 |
---|---|---|
DOCETAXEL(UNII: 15H5577CQD) (DOCETAXEL ANHYDROUS - UNII:699121PHCA) | DOCETAXEL ANHYDROUS | 80mg in 4 | 20mg in 1 |
Inactive Ingredients
Ingredient Name | Sanofi-Aventis U.S. LLC |
---|---|
ALCOHOL(3K9958V90M) | |
POLYSORBATE 80(6OZP39ZG8H) |
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