FdaApplication
ANDA 203912
Identifiers
- fda_app_no: ANDA203912
Properties
| Property | Value |
|---|---|
| applicant_name | NUKEMED INC DBA SPECTRONRX |
| application_type | ANDA |
| approval_date | 2015-04-22 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SODIUM FLUORIDE F-18 | SODIUM FLUORIDE F-18 | 10-200mCi/ML | INJECTABLE;INTRAVENOUS |
1 product