FdaApplication
NDA 017630
Identifiers
- fda_app_no: NDA017630
Properties
| Property | Value |
|---|---|
| applicant_name | GE HEALTHCARE |
| application_type | NDA |
| approval_date | 1993-01-08 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SODIUM IODIDE I 123 | SODIUM IODIDE I-123 | 200uCi | CAPSULE;ORAL |
| SODIUM IODIDE I 123 | SODIUM IODIDE I-123 | 100uCi | CAPSULE;ORAL |
| SODIUM IODIDE I 123 | SODIUM IODIDE I-123 | 2mCi/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | SOLUTION;ORAL |
3 products