FdaApplication
ANDA 215371
Identifiers
- fda_app_no: ANDA215371
Properties
| Property | Value |
|---|---|
| applicant_name | FRESENIUS KABI USA LLC |
| application_type | ANDA |
| approval_date | 2022-06-08 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MULTIPLE ELECTROLYTES INJECTION TYPE 1 USP PH 7.4 | MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE | 30MG/100ML;37MG/100ML;368MG/100ML;526MG/100ML;502MG/100ML | INJECTABLE;INJECTION |
1 product