FdaApplication
ANDA 072692
Identifiers
- fda_app_no: ANDA072692
Properties
| Property | Value |
|---|---|
| applicant_name | BARR LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1992-02-28 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NORTREL 0.5/35-21 | ETHINYL ESTRADIOL; NORETHINDRONE | 0.035MG;0.5MG | TABLET;ORAL-21 |
1 product