FdaApplication
ANDA 040702
Identifiers
- fda_app_no: ANDA040702
Properties
| Property | Value |
|---|---|
| applicant_name | LEADING PHARMA LLC |
| application_type | ANDA |
| approval_date | 2007-03-16 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| HYDROCHLOROTHIAZIDE | HYDROCHLOROTHIAZIDE | 50MG | TABLET;ORAL |
| HYDROCHLOROTHIAZIDE | HYDROCHLOROTHIAZIDE | 12.5MG | TABLET;ORAL |
| HYDROCHLOROTHIAZIDE | HYDROCHLOROTHIAZIDE | 25MG | TABLET;ORAL |
3 products