FdaApplication
ANDA 210088
Identifiers
- fda_app_no: ANDA210088
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2018-04-16 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LORATADINE | LORATADINE | 5MG | TABLET, CHEWABLE;ORAL |
| LORATADINE | LORATADINE | 10MG | TABLET, CHEWABLE;ORAL |
2 products