FdaApplication
ANDA 207769
Identifiers
- fda_app_no: ANDA207769
Properties
| Property | Value |
|---|---|
| applicant_name | ZYDUS PHARMACEUTICALS USA INC |
| application_type | ANDA |
| approval_date | 2018-05-24 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DUTASTERIDE AND TAMSULOSIN HYDROCHLORIDE | DUTASTERIDE; TAMSULOSIN HYDROCHLORIDE | 0.5MG;0.4MG | CAPSULE;ORAL |
1 product