FdaApplication
NDA 020204
Identifiers
- fda_app_no: NDA020204
Properties
| Property | Value |
|---|---|
| applicant_name | BAYER HEALTHCARE LLC |
| application_type | NDA |
| approval_date | 1994-01-11 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ALEVE | NAPROXEN SODIUM | 220MG | TABLET;ORAL |
1 product