FdaApplication
ANDA 204239
Identifiers
- fda_app_no: ANDA204239
Properties
| Property | Value |
|---|---|
| applicant_name | HETERO LABS LTD UNIT V |
| application_type | ANDA |
| approval_date | 2015-12-21 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LINEZOLID | LINEZOLID | 600MG | TABLET;ORAL |
1 product