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Serving leading biopharmaceutical companies globally:

McKinsey
Fuji
Deloitte
McKesson
QuintilesIMS
Mallinckrodt
Express Scripts
Daiichi Sankyo
Cipla
Novartis

Generated: January 16, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 202740

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NDA 202740 describes LEVONORGESTREL, which is a drug marketed by Wyeth Pharms Inc, Glenmark Pharms Ltd, Lotus Pharm Co Ltd, Lupin Ltd, Mylan Labs Ltd, Novel Labs Inc, Oc Pharma, Perrigo R And D, Reckitt Benckiser, Watson Labs, Watson Labs Inc, Amneal Pharms, Glenmark Generics, Mayne Pharma, and Barr, and is included in thirty-seven NDAs. It is available from fifteen suppliers. Additional details are available on the LEVONORGESTREL profile page.

The generic ingredient in LEVONORGESTREL is ethinyl estradiol; levonorgestrel. There are twenty-six drug master file entries for this compound. Twenty-six suppliers are listed for this compound. Additional details are available on the ethinyl estradiol; levonorgestrel profile page.
Summary for 202740
Tradename:LEVONORGESTREL
Applicant:Mylan Labs Ltd
Ingredient:levonorgestrel
Patents:0
Therapeutic Class:Hormonal Agents, Stimulant/Replacement/Modifying (Sex Hormones/Modifiers)
Formulation / Manufacturing:see details
Medical Subject Heading (MeSH) Categories for 202740

Profile for product number 001

Active Rx/OTC/Discontinued:OTCDosage:TABLET;ORALStrength0.75MG
Approval Date:Sep 2, 2016TE:RLD:No

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Serving leading biopharmaceutical companies globally:

Boehringer Ingelheim
Chubb
Novartis
Teva
US Department of Justice
Moodys
Daiichi Sankyo
Colorcon
Express Scripts

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