FdaApplication
NDA 017007
Identifiers
- fda_app_no: NDA017007
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA PHARMS |
| application_type | NDA |
Products (10)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| HEPARIN LOCK FLUSH | HEPARIN SODIUM | 10 UNITS/ML | INJECTABLE;INJECTION |
| HEPARIN LOCK FLUSH | HEPARIN SODIUM | 100 UNITS/ML | INJECTABLE;INJECTION |
| HEPARIN SODIUM | HEPARIN SODIUM | 5,000 UNITS/0.5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| HEPARIN SODIUM | HEPARIN SODIUM | 5,000 UNITS/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| HEPARIN SODIUM | HEPARIN SODIUM | 15,000 UNITS/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| HEPARIN SODIUM | HEPARIN SODIUM | 2,500 UNITS/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| HEPARIN SODIUM | HEPARIN SODIUM | 7,500 UNITS/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| HEPARIN SODIUM | HEPARIN SODIUM | 10,000 UNITS/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| HEPARIN SODIUM | HEPARIN SODIUM | 20,000 UNITS/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
| HEPARIN SODIUM | HEPARIN SODIUM | 1,000 UNITS/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INJECTION |
10 products