FdaApplication
ANDA 213584
Identifiers
- fda_app_no: ANDA213584
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | ANDA |
| approval_date | 2021-10-04 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| OXYMETAZOLINE HYDROCHLORIDE | OXYMETAZOLINE HYDROCHLORIDE | 1% | CREAM;TOPICAL |
1 product