FdaApplication
NDA 019229
Identifiers
- fda_app_no: NDA019229
Properties
| Property | Value |
|---|---|
| applicant_name | ABRAXIS PHARMACEUTICAL PRODUCTS |
| application_type | NDA |
| approval_date | 1987-05-05 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ZINC SULFATE | ZINC SULFATE | EQ 1MG ZINC/ML | INJECTABLE;INJECTION |
1 product