FdaApplication
ANDA 078682
Identifiers
- fda_app_no: ANDA078682
Properties
| Property | Value |
|---|---|
| applicant_name | BIONPHARMA INC |
| application_type | ANDA |
| approval_date | 2009-03-24 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IBUPROFEN | IBUPROFEN | EQ 200MG FREE ACID AND POTASSIUM SALT | CAPSULE;ORAL |
1 product