FdaApplication
NDA 006882
Identifiers
- fda_app_no: NDA006882
Properties
| Property | Value |
|---|---|
| applicant_name | SANOFI AVENTIS US LLC |
| application_type | NDA |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PHISOHEX | HEXACHLOROPHENE | 3% | EMULSION;TOPICAL |
1 product