FdaApplication
NDA 202832
Identifiers
- fda_app_no: NDA202832
Properties
| Property | Value |
|---|---|
| applicant_name | MEDEFIL INC |
| application_type | NDA |
| approval_date | 2012-01-06 |
Products (6)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SODIUM CHLORIDE 0.9% | SODIUM CHLORIDE | 9MG/ML (9MG/ML) | INJECTABLE;INJECTION |
| SODIUM CHLORIDE 0.9% | SODIUM CHLORIDE | 45MG/5ML (9MG/ML) | INJECTABLE;INJECTION |
| SODIUM CHLORIDE 0.9% | SODIUM CHLORIDE | 27MG/3ML (9MG/ML) | INJECTABLE;INJECTION |
| SODIUM CHLORIDE 0.9% | SODIUM CHLORIDE | 90MG/10ML (9MG/ML) | INJECTABLE;INJECTION |
| SODIUM CHLORIDE 0.9% | SODIUM CHLORIDE | 18MG/2ML (9MG/ML) | INJECTABLE;INJECTION |
| SODIUM CHLORIDE 0.9% | SODIUM CHLORIDE | 22.5MG/2.5ML (9MG/ML) | INJECTABLE;INJECTION |
6 products