FdaApplication
ANDA 070083
Identifiers
- fda_app_no: ANDA070083
Properties
| Property | Value |
|---|---|
| applicant_name | BASF CORP |
| application_type | ANDA |
| approval_date | 1985-02-22 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IBU | IBUPROFEN | 400MG | TABLET;ORAL |
1 product