FdaApplication
NDA 020449
Identifiers
- fda_app_no: NDA020449
Properties
| Property | Value |
|---|---|
| applicant_name | SANOFI AVENTIS US LLC |
| application_type | NDA |
| approval_date | 1996-05-14 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TAXOTERE | DOCETAXEL | 160MG/8ML (20MG/ML) | INJECTABLE;INJECTION |
| TAXOTERE | DOCETAXEL | 20MG/ML (20MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| TAXOTERE | DOCETAXEL | 40MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| TAXOTERE | DOCETAXEL | 80MG/4ML (20MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
4 products