FdaApplication
NDA 018897
Identifiers
- fda_app_no: NDA018897
Properties
| Property | Value |
|---|---|
| applicant_name | HOSPIRA INC |
| application_type | NDA |
| approval_date | 1984-07-20 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SODIUM CHLORIDE 14.6% | SODIUM CHLORIDE | 100MEQ/40ML (2.5MEQ/ML) | SOLUTION;INTRAVENOUS |
| SODIUM CHLORIDE 14.6% | SODIUM CHLORIDE | 50MEQ/20ML (2.5MEQ/ML) **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SOLUTION;INTRAVENOUS |
| SODIUM CHLORIDE 23.4% | SODIUM CHLORIDE | 400MEQ/100ML (4MEQ/ML) | SOLUTION;INTRAVENOUS |
3 products