BioPharmaceutical Business Intelligence

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Serving leading biopharmaceutical companies globally:

Merck
AstraZeneca
Healthtrust
Moodys
Mallinckrodt
Colorcon
Daiichi Sankyo
Boehringer Ingelheim
Farmers Insurance
Covington

Generated: January 19, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 072921

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NDA 072921 describes PRAZOSIN HYDROCHLORIDE, which is a drug marketed by Am Therap, Dava Pharms Inc, Idt Australia Ltd, Mylan, Purepac Pharm, Teva Pharms, and Watson Labs, and is included in fifteen NDAs. It is available from twelve suppliers. Additional details are available on the PRAZOSIN HYDROCHLORIDE profile page.

The generic ingredient in PRAZOSIN HYDROCHLORIDE is prazosin hydrochloride. There are sixteen drug master file entries for this compound. Fourteen suppliers are listed for this compound. Additional details are available on the prazosin hydrochloride profile page.
Summary for 072921
Tradename:PRAZOSIN HYDROCHLORIDE
Applicant:Purepac Pharm
Ingredient:prazosin hydrochloride
Patents:0
Therapeutic Class:Cardiovascular Agents
Genitourinary Agents
Formulation / Manufacturing:see details
Medical Subject Heading (MeSH) Categories for 072921

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:CAPSULE;ORALStrengthEQ 2MG BASE
Approval Date:May 16, 1989TE:RLD:No

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Serving leading biopharmaceutical companies globally:

Argus Health
US Department of Justice
Novartis
Baxter
Teva
Julphar
AstraZeneca
UBS
McKinsey

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