FdaApplication
ANDA 076557
Identifiers
- fda_app_no: ANDA076557
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2004-09-22 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LORATADINE AND PSEUDOEPHEDRINE SULFATE | LORATADINE; PSEUDOEPHEDRINE SULFATE | 10MG;240MG | TABLET, EXTENDED RELEASE;ORAL |
1 product