FdaApplication
ANDA 209641
Identifiers
- fda_app_no: ANDA209641
Properties
| Property | Value |
|---|---|
| applicant_name | ACTAVIS LABORATORIES UT INC INDIRECT WHOLLY OWNED SUB OF TEVA PHARMACEUTICALS USA INC |
| application_type | ANDA |
| approval_date | 2022-06-22 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ADAPALENE AND BENZOYL PEROXIDE | ADAPALENE; BENZOYL PEROXIDE | 0.3%;2.5% | GEL;TOPICAL |
1 product