FdaApplication
NDA 018197
Identifiers
- fda_app_no: NDA018197
Properties
| Property | Value |
|---|---|
| applicant_name | BASF CORP |
| application_type | NDA |
| approval_date | 1984-03-05 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IBU | IBUPROFEN | 400MG | TABLET;ORAL |
| RUFEN | IBUPROFEN | 600MG | TABLET;ORAL |
2 products