PHEXXI (LACTIC ACID, L-, CITRIC ACID MONOHYDRATE, AND POTASSIUM BITARTRATE)
Summary
FDA approved PHEXXI (LACTIC ACID, L-, CITRIC ACID MONOHYDRATE, AND POTASSIUM BITARTRATE) by EVOFEM INC. NDA (New Drug) approval (Labeling) on 2025-04-21. GEL, VAGINAL.
Details
Source
Drug Approval
External ID
NDA208352-5
Action Date
2025-04-21
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
PHEXXI (generic: LACTIC ACID, L-, CITRIC ACID MONOHYDRATE, AND POTASSIUM BITARTRATE), GEL, VAGINAL. Application: NDA208352
Company
Context & Analysis
EVOFEM INC has 2 FDA actions in our database.
Frequently Asked Questions
How often does EVOFEM INC have FDA actions?
EVOFEM INC has 2 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA208352-5" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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