FdaApplication
ANDA 206569
Identifiers
- fda_app_no: ANDA206569
Properties
| Property | Value |
|---|---|
| applicant_name | PHARMOBEDIENT CONSULTING LLC |
| application_type | ANDA |
| approval_date | 2018-11-27 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TENOFOVIR DISOPROXIL FUMARATE | TENOFOVIR DISOPROXIL FUMARATE | 200MG | TABLET;ORAL |
| TENOFOVIR DISOPROXIL FUMARATE | TENOFOVIR DISOPROXIL FUMARATE | 300MG | TABLET;ORAL |
| TENOFOVIR DISOPROXIL FUMARATE | TENOFOVIR DISOPROXIL FUMARATE | 250MG | TABLET;ORAL |
| TENOFOVIR DISOPROXIL FUMARATE | TENOFOVIR DISOPROXIL FUMARATE | 150MG | TABLET;ORAL |
4 products