FdaApplication
ANDA 217190
Identifiers
- fda_app_no: ANDA217190
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | ANDA |
| approval_date | 2025-05-02 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| HALOBETASOL PROPIONATE AND TAZAROTENE | HALOBETASOL PROPIONATE; TAZAROTENE | 0.01%;0.045% | LOTION;TOPICAL |
1 product