FdaApplication
ANDA 078688
Identifiers
- fda_app_no: ANDA078688
Properties
| Property | Value |
|---|---|
| applicant_name | NATCO PHARMA LTD |
| application_type | ANDA |
| approval_date | 2008-02-15 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NADOLOL AND BENDROFLUMETHIAZIDE | BENDROFLUMETHIAZIDE; NADOLOL | 5MG;40MG | TABLET;ORAL |
| NADOLOL AND BENDROFLUMETHIAZIDE | BENDROFLUMETHIAZIDE; NADOLOL | 5MG;80MG | TABLET;ORAL |
2 products