FEMLYV (NORETHINDRONE ACETATE/ETHINYL ESTRADIOL)
Summary
FDA approved FEMLYV (NORETHINDRONE ACETATE/ETHINYL ESTRADIOL) by MILLICENT PR. NDA (New Drug) approval (Labeling) on 2025-07-29. TABLET, ORALLY DISINTEGRATING, ORAL.
Details
Source
Drug Approval
External ID
NDA218718-1
Action Date
2025-07-29
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
FEMLYV (generic: NORETHINDRONE ACETATE/ETHINYL ESTRADIOL), TABLET, ORALLY DISINTEGRATING, ORAL. Application: NDA218718
Company
Context & Analysis
Frequently Asked Questions
How often does MILLICENT PR have FDA actions?
This is the only FDA action we have on record for MILLICENT PR in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA218718-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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