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Serving leading biopharmaceutical companies globally:

Chubb
Fish and Richardson
Daiichi Sankyo
Accenture
Teva
Deloitte
Chinese Patent Office
Federal Trade Commission
Covington
Citi

Generated: February 20, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 084417

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NDA 084417 describes PREDNISONE, which is a drug marketed by West-ward Pharms Int, Wockhardt, Actavis Labs Fl Inc, Am Therap, Amneal Pharms Ny, Aurolife Pharma Llc, Bundy, Chartwell Rx, Contract Pharmacal, Duramed Pharms Barr, Elkins Sinn, Everylife, Ferrante, Halsey, Heather, Hikma Pharms, Impax Labs, Inwood Labs, Ivax Sub Teva Pharms, Jubilant Cadista, Kv Pharm, Lannett, Lederle, Marshall Pharma, Mutual Pharm, Mylan Pharms Inc, Nylos, Panray, Pharmavite, Phoenix Labs Ny, Purepac Pharm, Pvt Form, Rexall, Roxane, Sandoz, Scherer Labs, Sperti, Sun Pharm Industries, Superpharm, Teva, UDL, Upsher Smith, Valeant Pharm Intl, Vangard, Vintage Pharms, Vitarine, Watson Labs, and Whiteworth Town Plsn, and is included in one hundred and seven NDAs. It is available from fifty-nine suppliers. Additional details are available on the PREDNISONE profile page.

The generic ingredient in PREDNISONE is prednisone. There are sixteen drug master file entries for this compound. Sixty suppliers are listed for this compound. Additional details are available on the prednisone profile page.
Summary for 084417
Tradename:PREDNISONE
Applicant:Heather
Ingredient:prednisone
Patents:0
Therapeutic Class:Hormonal Agents, Stimulant/Replacement/Modifying (Adrenal)
Inflammatory Bowel Disease Agents
Formulation / Manufacturing:see details
Medical Subject Heading (MeSH) Categories for 084417

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength20MG
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

AstraZeneca
McKesson
Harvard Business School
Fish and Richardson
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Deloitte
Johnson and Johnson
McKinsey
Express Scripts

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