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Serving hundreds of leading biopharmaceutical companies globally:

AstraZeneca
Merck
Fuji
Dow
Teva
Julphar
Chubb
Cerilliant
Healthtrust

Generated: May 21, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 070747

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NDA 070747 describes CLONIDINE HYDROCHLORIDE, which is a drug marketed by Exela Pharma Scs Llc, Fresenius Kabi Usa, Hikma Farmaceutica, Luitpold, Zydus Pharms Usa Inc, Actavis Elizabeth, Ajanta Pharma Ltd, Amneal Pharms Ny, Anchen Pharms, Jubilant Generics, Lupin Ltd, Mayne Pharma Inc, Xiamen Lp Pharm Co, Alembic Pharms Ltd, Am Therap, Aurolife Pharma Llc, Chartwell Molecules, Duramed Pharms Barr, Frontida Biopharm, Impax Labs, Interpharm, Mylan, Par Pharm, Prinston Inc, Sun Pharm Inds Inc, Teva, Unichem, Warner Chilcott, Watson Labs, and Yung Shin Pharm, and is included in fifty-seven NDAs. It is available from sixty-four suppliers. Additional details are available on the CLONIDINE HYDROCHLORIDE profile page.

The generic ingredient in CLONIDINE HYDROCHLORIDE is chlorthalidone; clonidine hydrochloride. There are nineteen drug master file entries for this compound. Additional details are available on the chlorthalidone; clonidine hydrochloride profile page.
Summary for 070747
Tradename:CLONIDINE HYDROCHLORIDE
Applicant:Teva
Ingredient:clonidine hydrochloride
Patents:0
Therapeutic Class:Cardiovascular Agents
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength0.1MG
Approval Date:Jul 8, 1986TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

McKinsey
McKesson
Johnson and Johnson
Fish and Richardson
Fuji
Chinese Patent Office
Cerilliant
AstraZeneca
Farmers Insurance

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