LO LOESTRIN FE (NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL, ETHINYL ESTRADIOL AND FERROUS FUMARATE)
Summary
FDA approved LO LOESTRIN FE (NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL, ETHINYL ESTRADIOL AND FERROUS FUMARATE) by APIL. NDA (New Drug) approval (Labeling) on 2022-04-29. TABLET, ORAL.
Details
Source
Drug Approval
External ID
NDA022501-15
Action Date
2022-04-29
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
LO LOESTRIN FE (generic: NORETHINDRONE ACETATE AND ETHINYL ESTRADIOL, ETHINYL ESTRADIOL AND FERROUS FUMARATE), TABLET, ORAL. Application: NDA022501
Company
Context & Analysis
APIL has 4 FDA actions in our database.
Frequently Asked Questions
How often does APIL have FDA actions?
APIL has 4 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 "NDA022501-15" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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