FdaApplication
NDA 208352
Identifiers
- fda_app_no: NDA208352
Properties
| Property | Value |
|---|---|
| applicant_name | EVOFEM INC |
| application_type | NDA |
| approval_date | 2020-05-22 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PHEXX | CITRIC ACID; LACTIC ACID; POTASSIUM BITARTRATE | 1%;1.8%;0.4% | GEL;VAGINAL |
1 product