FdaApplication
ANDA 210549
Identifiers
- fda_app_no: ANDA210549
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | ANDA |
| approval_date | 2019-08-23 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AZELAIC ACID | AZELAIC ACID | 15% | GEL;TOPICAL |
1 product