FdaApplication
ANDA 077101
Identifiers
- fda_app_no: ANDA077101
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 2006-09-06 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| QUASENSE | ETHINYL ESTRADIOL; LEVONORGESTREL | 0.03MG;0.15MG | TABLET;ORAL |
1 product