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Profile for Tradename: LOESTRIN 24 FE

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Loestrin 24 Fe is a drug marketed by Warner Chilcott and is included in one NDA. It is available from two suppliers. There is one patent protecting this drug and one Paragraph IV challenge.

The generic ingredient in LOESTRIN 24 FE is ethinyl estradiol; norethindrone acetate. There are twenty-six drug master file entries for this compound. Four suppliers are listed for this compound. Additional details are available on the ethinyl estradiol; norethindrone acetate profile page.

Summary for Tradename: LOESTRIN 24 FE

Patents:1
Applicants:1
NDAs:1
Suppliers / Packagers: see list4
Formulation / Manufacturing:see details

Clinical Trials for: LOESTRIN 24 FE

Study of Loestrin 24(24 Days of "Real" Pills) Fe Versus Loestrin 1/20 (21 "Real" Pills)
Status: Completed Condition: Pelvic Pain; Headaches; Emotional

Post Operative Continuous Active Combination Sex Steroids for the Prevention of Recurrent Endometrioma Formation
Status: Withdrawn Condition: Endometrioma

Study of the Contraceptive Efficacy and Safety of a NOMAC-E2 Combined Oral Contraceptive (COC)(P06448)
Status: Terminated Condition: Contraception

Courtesy of ClinicalTrials.org
See more clinical trials for this drug
Applicant Tradename Generic Name Dosage NDA Approval Date Type RLD Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Warner Chilcott
LOESTRIN 24 FE
ethinyl estradiol; norethindrone acetate
TABLET;ORAL021871-001Feb 17, 2006DISCNNo5,552,394<disabled><disabled>
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Paragraph IV activity for: LOESTRIN 24 FE

Drugname Dosage Strength RLD Submissiondate
norethindrone acetate/ ethinyl estradiol and ferrous fumarateTablets1 mg/0.02 mg and 75 mgLoestrin 24 Fe4/17/2006
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ISSN: 2162-2639

Preferred citation:

Friedman, Y. Location of pharmaceutical innovation: 2000–2009 Nature Reviews Drug Discovery 9, 835–836 (2010).

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