JUNEL FE 28 DAY (NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL AND FERROUS FUMARATE)
Summary
FDA approved JUNEL FE 28 DAY (NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL AND FERROUS FUMARATE) by BARR. ANDA (Generic) approval (Labeling) on 2023-09-25. TABLET, ORAL-28.
Details
Source
Drug Approval
External ID
ANDA076064-26
Action Date
2023-09-25
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
JUNEL FE 28 DAY (generic: NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL AND FERROUS FUMARATE), TABLET, ORAL-28. Application: ANDA076064
Company
Context & Analysis
BARR has 16 FDA actions in our database.
Frequently Asked Questions
How often does BARR have FDA actions?
BARR has 16 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 "ANDA076064-26" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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