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Serving leading biopharmaceutical companies globally:

Cerilliant
Accenture
Julphar
Queensland Health
Medtronic
Johnson and Johnson
Novartis
Federal Trade Commission
Cantor Fitzgerald
Argus Health

Generated: January 24, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 070702

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NDA 070702 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, Anchen Pharms, Lupin Ltd, 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-four NDAs. It is available from sixty suppliers. Additional details are available on the CLONIDINE HYDROCHLORIDE profile page.

The generic ingredient in CLONIDINE HYDROCHLORIDE is chlorthalidone; clonidine hydrochloride. There are eighteen drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the chlorthalidone; clonidine hydrochloride profile page.
Summary for 070702
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;ORALStrength0.2MG
Approval Date:Jul 8, 1986TE:RLD:No

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Serving leading biopharmaceutical companies globally:

Queensland Health
Chubb
US Army
Harvard Business School
UBS
Citi
Novartis
Baxter
Johnson and Johnson

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