FdaApplication
ANDA 208740
Identifiers
- fda_app_no: ANDA208740
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | ANDA |
| approval_date | 2021-06-16 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE | EMTRICITABINE; TENOFOVIR DISOPROXIL FUMARATE | 200MG;300MG | TABLET;ORAL |
1 product