AZURETTE (DESOGESTREL/ETHINYL ESTRADIOL AND ETHINYL ESTRADIOL)
Summary
FDA approved AZURETTE (DESOGESTREL/ETHINYL ESTRADIOL AND ETHINYL ESTRADIOL) by NOVAST LABS. ANDA (Generic) approval (Labeling) on 2024-07-08. TABLET, ORAL-28.
Details
Source
Drug Approval
External ID
ANDA091247-10
Action Date
2024-07-08
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
AZURETTE (generic: DESOGESTREL/ETHINYL ESTRADIOL AND ETHINYL ESTRADIOL), TABLET, ORAL-28. Application: ANDA091247
Company
Context & Analysis
NOVAST LABS has 14 FDA actions in our database.
Frequently Asked Questions
How often does NOVAST LABS have FDA actions?
NOVAST LABS has 14 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 "ANDA091247-10" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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