VYFEMLA (NORETHINDRONE AND ETHINYL ESTRADIOL)
Summary
FDA approved VYFEMLA (NORETHINDRONE AND ETHINYL ESTRADIOL) by LUPIN. ANDA (Generic) approval (Labeling) on 2022-04-29. TABLET, ORAL-28.
Details
Source
Drug Approval
External ID
ANDA201886-10
Action Date
2022-04-29
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
VYFEMLA (generic: NORETHINDRONE AND ETHINYL ESTRADIOL), TABLET, ORAL-28. Application: ANDA201886
Company
Context & Analysis
LUPIN has 61 FDA actions in our database.
Frequently Asked Questions
How often does LUPIN have FDA actions?
LUPIN has 61 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 "ANDA201886-10" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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