FdaApplication
ANDA 212114
Identifiers
- fda_app_no: ANDA212114
Properties
| Property | Value |
|---|---|
| applicant_name | LAURUS LABS LTD |
| application_type | ANDA |
| approval_date | 2019-07-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE | EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE | 200MG;300MG | TABLET;ORAL |
1 product