FdaApplication
ANDA 202988
Identifiers
- fda_app_no: ANDA202988
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2019-02-06 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SYLEVIA | ETHINYL ESTRADIOL; LEVONORGESTREL | 0.03MG;0.15MG | TABLET;ORAL |
1 product