FdaApplication
ANDA 206694
Identifiers
- fda_app_no: ANDA206694
Properties
| Property | Value |
|---|---|
| applicant_name | ZYDUS PHARMACEUTICALS USA INC |
| application_type | ANDA |
| approval_date | 2017-10-27 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TAMOXIFEN CITRATE | TAMOXIFEN CITRATE | EQ 20MG BASE | TABLET;ORAL |
| TAMOXIFEN CITRATE | TAMOXIFEN CITRATE | EQ 10MG BASE | TABLET;ORAL |
2 products