FdaApplication
ANDA 207095
Identifiers
- fda_app_no: ANDA207095
Properties
| Property | Value |
|---|---|
| applicant_name | SHANDONG XINHUA PHARMACEUTICAL CO LTD |
| application_type | ANDA |
| approval_date | 2017-05-05 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IBUPROFEN | IBUPROFEN | 200MG | TABLET;ORAL |
| IBUPROFEN | IBUPROFEN | 200MG | TABLET;ORAL |
2 products