FdaApplication
ANDA 218182
Identifiers
- fda_app_no: ANDA218182
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | ANDA |
| approval_date | 2023-12-07 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LIDOCAINE HYDROCHLORIDE | LIDOCAINE HYDROCHLORIDE | 4% | SOLUTION;TOPICAL |
1 product