FdaApplication
ANDA 217796
Identifiers
- fda_app_no: ANDA217796
Properties
| Property | Value |
|---|---|
| applicant_name | FRESENIUS KABI USA LLC |
| application_type | ANDA |
| approval_date | 2023-07-11 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SODIUM CHLORIDE 23.4% | SODIUM CHLORIDE | 234MG/ML | INJECTABLE;INJECTION |
1 product