FdaApplication
ANDA 205072
Identifiers
- fda_app_no: ANDA205072
Properties
| Property | Value |
|---|---|
| applicant_name | CSPC OUYI PHARMACEUTICAL CO LTD |
| application_type | ANDA |
| approval_date | 2017-07-28 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CEFADROXIL | CEFADROXIL/CEFADROXIL HEMIHYDRATE | EQ 500MG BASE | CAPSULE;ORAL |
1 product