FdaApplication
ANDA 206687
Identifiers
- fda_app_no: ANDA206687
Properties
| Property | Value |
|---|---|
| applicant_name | FRESENIUS KABI USA LLC |
| application_type | ANDA |
| approval_date | 2017-10-30 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SODIUM ACETATE | SODIUM ACETATE | 400MEQ/100ML (4MEQ/ML) | SOLUTION;INTRAVENOUS |
1 product