PREFEST
Summary
FDA approved PREFEST by TEVA WOMENS. NDA (New Drug) approval (Labeling) on 2024-02-15. TABLET, ORAL.
Details
Source
Drug Approval
External ID
NDA021040-15
Action Date
2024-02-15
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
PREFEST, TABLET, ORAL. Application: NDA021040
Company
Context & Analysis
TEVA WOMENS has 2 FDA actions in our database.
Frequently Asked Questions
How often does TEVA WOMENS have FDA actions?
TEVA WOMENS 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 "NDA021040-15" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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