FdaApplication
ANDA 206581
Identifiers
- fda_app_no: ANDA206581
Properties
| Property | Value |
|---|---|
| applicant_name | PERRIGO R AND D CO |
| application_type | ANDA |
| approval_date | 2015-08-03 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| IBUPROFEN SODIUM | IBUPROFEN SODIUM | EQ 200MG BASE | TABLET;ORAL |
1 product