FdaApplication
ANDA 206959
Identifiers
- fda_app_no: ANDA206959
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | ANDA |
| approval_date | 2018-01-24 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ADAPALENE AND BENZOYL PEROXIDE | ADAPALENE; BENZOYL PEROXIDE | 0.1%;2.5% | GEL;TOPICAL |
1 product