FdaApplication
ANDA 207001
Identifiers
- fda_app_no: ANDA207001
Properties
| Property | Value |
|---|---|
| applicant_name | HQ SPECIALTY PHARMA CORP |
| application_type | ANDA |
| approval_date | 2017-07-07 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LINEZOLID | LINEZOLID | 600MG/300ML (2MG/ML) | SOLUTION;INTRAVENOUS |
| LINEZOLID | LINEZOLID | 200MG/100ML (2MG/ML) | SOLUTION;INTRAVENOUS |
2 products