FdaApplication
ANDA 212070
Identifiers
- fda_app_no: ANDA212070
Properties
| Property | Value |
|---|---|
| applicant_name | FRESENIUS KABI USA LLC |
| application_type | ANDA |
| approval_date | 2021-04-28 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SODIUM CHLORIDE 14.6% | SODIUM CHLORIDE | 50MEQ/20ML (2.5MEQ/ML) | SOLUTION;INTRAVENOUS |
| SODIUM CHLORIDE 14.6% | SODIUM CHLORIDE | 100MEQ/40ML (2.5MEQ/ML) | SOLUTION;INTRAVENOUS |
| SODIUM CHLORIDE 23.4% | SODIUM CHLORIDE | 400MEQ/100ML (4MEQ/ML) | SOLUTION;INTRAVENOUS |
3 products