FdaApplication
NDA 020452
Identifiers
- fda_app_no: NDA020452
Properties
| Property | Value |
|---|---|
| applicant_name | CORDENPHARMA |
| application_type | NDA |
| approval_date | 2003-07-14 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PARAPLATIN | CARBOPLATIN | 450MG/45ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INTRAVENOUS |
| PARAPLATIN | CARBOPLATIN | 50MG/5ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INTRAVENOUS |
| PARAPLATIN | CARBOPLATIN | 150MG/15ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INTRAVENOUS |
| PARAPLATIN | CARBOPLATIN | 600MG/60ML (10MG/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INTRAVENOUS |
4 products