FdaApplication
ANDA 206171
Identifiers
- fda_app_no: ANDA206171
Properties
| Property | Value |
|---|---|
| applicant_name | SPECTRA MEDICAL DEVICES INC |
| application_type | ANDA |
| approval_date | 2017-07-21 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SODIUM CHLORIDE 0.9% | SODIUM CHLORIDE | 45MG/5ML (9MG/ML) | SOLUTION;INJECTION |
| SODIUM CHLORIDE 0.9% | SODIUM CHLORIDE | 90MG/10ML (9MG/ML) | SOLUTION;INJECTION |
2 products