FdaApplication
ANDA 202413
Identifiers
- fda_app_no: ANDA202413
Properties
| Property | Value |
|---|---|
| applicant_name | SHANDONG XINHUA PHARMACEUTICAL CO LTD |
| application_type | ANDA |
| approval_date | 2016-11-23 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IBUPROFEN | IBUPROFEN | 400MG | TABLET;ORAL |
| IBUPROFEN | IBUPROFEN | 300MG | TABLET;ORAL |
| IBUPROFEN | IBUPROFEN | 800MG | TABLET;ORAL |
| IBUPROFEN | IBUPROFEN | 600MG | TABLET;ORAL |
4 products