FdaApplication
NDA 202317
Identifiers
- fda_app_no: NDA202317
Properties
| Property | Value |
|---|---|
| applicant_name | HELSINN BIREX PHARMACEUTICALS LTD |
| application_type | NDA |
| approval_date | 2013-08-23 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VALCHLOR | MECHLORETHAMINE HYDROCHLORIDE | EQ 0.016% BASE | GEL;TOPICAL |
1 product