FdaApplication
NDA 018803
Identifiers
- fda_app_no: NDA018803
Properties
| Property | Value |
|---|---|
| applicant_name | HOSPIRA INC |
| application_type | NDA |
| approval_date | 1982-10-29 |
Products (6)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | SODIUM CHLORIDE | 45MG/5ML (9MG/ML) | SOLUTION;INJECTION |
| SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | SODIUM CHLORIDE | 90MG/10ML (9MG/ML) | SOLUTION;INJECTION |
| SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | SODIUM CHLORIDE | 450MG/50ML (9MG/ML) | SOLUTION;INJECTION |
| SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | SODIUM CHLORIDE | 27MG/3ML (9MG/ML) | SOLUTION;INJECTION |
| SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | SODIUM CHLORIDE | 18MG/2ML (9MG/ML) | SOLUTION;INJECTION |
| SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | SODIUM CHLORIDE | 180MG/20ML (9MG/ML) | SOLUTION;INJECTION |
6 products