FdaApplication
NDA 017378
Identifiers
- fda_app_no: NDA017378
Properties
| Property | Value |
|---|---|
| applicant_name | BAXTER HEALTHCARE CORP |
| application_type | NDA |
| approval_date | 1982-11-22 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PLASMA-LYTE 148 IN WATER IN PLASTIC CONTAINER | MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE | 30MG/100ML;37MG/100ML;368MG/100ML;526MG/100ML;502MG/100ML | INJECTABLE;INJECTION |
| PLASMA-LYTE A IN PLASTIC CONTAINER | MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE | 30MG/100ML;37MG/100ML;368MG/100ML;526MG/100ML;502MG/100ML | INJECTABLE;INJECTION |
2 products