FdaApplication
NDA 020212
Identifiers
- fda_app_no: NDA020212
Properties
| Property | Value |
|---|---|
| applicant_name | PFIZER INC |
| application_type | NDA |
| approval_date | 1995-05-26 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ZINECARD | DEXRAZOXANE HYDROCHLORIDE | EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| ZINECARD | DEXRAZOXANE HYDROCHLORIDE | EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
2 products