FdaApplication
NDA 201803
Identifiers
- fda_app_no: NDA201803
Properties
| Property | Value |
|---|---|
| applicant_name | HALEON US HOLDINGS LLC |
| application_type | NDA |
| approval_date | 2012-06-12 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ADVIL | IBUPROFEN SODIUM | EQ 200MG BASE | TABLET;ORAL |
1 product