Product NDC: | 0075-8005 |
Proprietary Name: | TAXOTERE |
Non Proprietary Name: | Docetaxel |
Active Ingredient(s): | 80 mg/4mL & nbsp; Docetaxel |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION, CONCENTRATE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0075-8005 |
Labeler Name: | sanofi-aventis U.S. LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020449 |
Marketing Category: | NDA |
Start Marketing Date: | 20100802 |
Package NDC: | 0075-8005-01 |
Package Description: | 1 VIAL, GLASS in 1 CARTON (0075-8005-01) > 8 mL in 1 VIAL, GLASS |
NDC Code | 0075-8005-01 |
Proprietary Name | TAXOTERE |
Package Description | 1 VIAL, GLASS in 1 CARTON (0075-8005-01) > 8 mL in 1 VIAL, GLASS |
Product NDC | 0075-8005 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Docetaxel |
Dosage Form Name | INJECTION, SOLUTION, CONCENTRATE |
Route Name | INTRAVENOUS |
Start Marketing Date | 20100802 |
Marketing Category Name | NDA |
Labeler Name | sanofi-aventis U.S. LLC |
Substance Name | DOCETAXEL |
Strength Number | 80 |
Strength Unit | mg/4mL |
Pharmaceutical Classes |