FdaApplication
NDA 019217
Identifiers
- fda_app_no: NDA019217
Properties
| Property | Value |
|---|---|
| applicant_name | ICU MEDICAL INC |
| application_type | NDA |
| approval_date | 1984-07-13 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | SODIUM CHLORIDE | 360MG/40ML (9MG/ML) | SOLUTION;INJECTION |
| 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 THERMOJECT KIT FOR CARDIAC OUTPUT USE | SODIUM CHLORIDE | 90MG/10ML (9MG/ML) | SOLUTION;INJECTION |
4 products