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Citi
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Harvard Business School
Medtronic
Dow
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Covington

Generated: June 22, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 017354

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NDA 017354 describes LOESTRIN FE 1/20, which is a drug marketed by Apil and is included in one NDA. It is available from two suppliers. Additional details are available on the LOESTRIN FE 1/20 profile page.

The generic ingredient in LOESTRIN FE 1/20 is ethinyl estradiol; norethindrone acetate. There are twenty-six drug master file entries for this compound. Twenty-one suppliers are listed for this compound. Additional details are available on the ethinyl estradiol; norethindrone acetate profile page.
Summary for 017354
Tradename:LOESTRIN FE 1/20
Applicant:Apil
Ingredient:ethinyl estradiol; norethindrone acetate
Patents:0
Formulation / Manufacturing:see details
Suppliers and Packaging for NDA: 017354
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
LOESTRIN FE 1/20 ethinyl estradiol; norethindrone acetate TABLET;ORAL-28 017354 NDA AUTHORIZED GENERIC Mayne Pharma Inc. 51862-012 N 51862-012-06
LOESTRIN FE 1/20 ethinyl estradiol; norethindrone acetate TABLET;ORAL-28 017354 NDA AUTHORIZED GENERIC Actavis Pharma, Inc. 52544-249 N 52544-249-28

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORAL-28Strength0.02MG;1MG
Approval Date:Approved Prior to Jan 1, 1982TE:ABRLD:Yes

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Serving hundreds of leading biopharmaceutical companies globally:

Baxter
Harvard Business School
Daiichi Sankyo
Cantor Fitzgerald
Express Scripts
Covington
Merck
Argus Health
Accenture

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