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Serving leading biopharmaceutical companies globally:

Julphar
Cantor Fitzgerald
Medtronic
Farmers Insurance
Federal Trade Commission
AstraZeneca
US Army
Accenture
Harvard Business School
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Generated: January 18, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 070887

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NDA 070887 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 sixteen 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 070887
Tradename:CLONIDINE HYDROCHLORIDE
Applicant:Aurolife Pharma Llc
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:Aug 31, 1988TE:RLD:No

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Serving leading biopharmaceutical companies globally:

Accenture
Moodys
Fuji
Cerilliant
McKesson
Julphar
Federal Trade Commission
Queensland Health
Farmers Insurance

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