FdaApplication
NDA 019329
Identifiers
- fda_app_no: NDA019329
Properties
| Property | Value |
|---|---|
| applicant_name | ABRAXIS PHARMACEUTICAL PRODUCTS |
| application_type | NDA |
| approval_date | 1987-04-22 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SODIUM CHLORIDE 23.4% IN PLASTIC CONTAINER | SODIUM CHLORIDE | 234MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
1 product