FdaApplication
ANDA 217261
Identifiers
- fda_app_no: ANDA217261
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | ANDA |
| approval_date | 2023-08-08 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IBUPROFEN | IBUPROFEN | 40MG/ML | SUSPENSION/DROPS;ORAL |
1 product