 
				 
										
USFDA APPLICATION NUMBER - 20449 / DOSAGE - INJECTABLE;INJECTION - 80MG/4ML (20MG/ML)
| 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 | Actavis Pharma, Inc. | Hikma Pharmaceuticals USA Inc. | McKesson Packaging Services a business unit of McKesson Corporation | Northstar RxLLC | Sagent Pharmaceuticals | Sanofi-Aventis U.S. LLC | Teva Parenteral Medicines, Inc. | Jiangsu Hengrui Pharmaceuticals Co., Ltd. | 
|---|---|---|---|---|---|---|---|---|
| ALCOHOL(3K9958V90M) | ||||||||
| ANHYDROUS CITRIC ACID(XF417D3PSL) | ||||||||
| POLYSORBATE 80(6OZP39ZG8H) | ||||||||
| povidone k12(333AG72FWJ) |