FdaApplication
ANDA 073582
Identifiers
- fda_app_no: ANDA073582
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES INC |
| application_type | ANDA |
| approval_date | 1993-04-29 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ATENOLOL AND CHLORTHALIDONE | ATENOLOL; CHLORTHALIDONE | 50MG;25MG | TABLET;ORAL |
| ATENOLOL AND CHLORTHALIDONE | ATENOLOL; CHLORTHALIDONE | 100MG;25MG | TABLET;ORAL |
2 products