FdaApplication
ANDA 070783
Identifiers
- fda_app_no: ANDA070783
Properties
| Property | Value |
|---|---|
| applicant_name | PAR PHARMACEUTICAL INC |
| application_type | ANDA |
| approval_date | 1987-11-06 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| METHYLDOPA AND CHLOROTHIAZIDE | CHLOROTHIAZIDE; METHYLDOPA | 150MG;250MG | TABLET;ORAL |
1 product