FdaApplication
ANDA 072722
Identifiers
- fda_app_no: ANDA072722
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1991-12-30 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ZOVIA 1/50E-21 | ETHINYL ESTRADIOL; ETHYNODIOL DIACETATE | 0.05MG;1MG | TABLET;ORAL-21 |
1 product