FdaApplication
NDA 018609
Identifiers
- fda_app_no: NDA018609
Properties
| Property | Value |
|---|---|
| applicant_name | BAXTER HEALTHCARE CORP |
| application_type | NDA |
| approval_date | 1982-04-28 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| HEPARIN SODIUM 1,000 UNITS AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | HEPARIN SODIUM | 200 UNITS/100ML | INJECTABLE;INJECTION |
| HEPARIN SODIUM 2,000 UNITS AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | HEPARIN SODIUM | 200 UNITS/100ML | INJECTABLE;INJECTION |
| HEPARIN SODIUM 2,000 UNITS AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | HEPARIN SODIUM | 2,000 UNITS/1000ML | INJECTABLE;INJECTION |
| HEPARIN SODIUM 5,000 UNITS AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER | HEPARIN SODIUM | 500 UNITS/100ML | INJECTABLE;INJECTION |
4 products