FdaApplication
NDA 021734
Identifiers
- fda_app_no: NDA021734
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | NDA |
| approval_date | 2005-10-04 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LORATADINE | LORATADINE | 1MG/ML | SUSPENSION;ORAL |
1 product