Product NDC: | 0075-8001 |
Proprietary Name: | Taxotere |
Non Proprietary Name: | docetaxel |
Active Ingredient(s): | 40 mg/mL & nbsp; docetaxel |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0075-8001 |
Labeler Name: | sanofi-aventis U.S. LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020449 |
Marketing Category: | NDA |
Start Marketing Date: | 20100515 |
Package NDC: | 0075-8001-20 |
Package Description: | .5 mL in 1 VIAL, GLASS (0075-8001-20) |
NDC Code | 0075-8001-20 |
Proprietary Name | Taxotere |
Package Description | .5 mL in 1 VIAL, GLASS (0075-8001-20) |
Product NDC | 0075-8001 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | docetaxel |
Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
Route Name | INTRAVENOUS |
Start Marketing Date | 20100515 |
Marketing Category Name | NDA |
Labeler Name | sanofi-aventis U.S. LLC |
Substance Name | DOCETAXEL |
Strength Number | 40 |
Strength Unit | mg/mL |
Pharmaceutical Classes |