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Serving hundreds of leading biopharmaceutical companies globally:

US Army
McKinsey
Express Scripts
Argus Health
Boehringer Ingelheim
US Department of Justice
QuintilesIMS
Colorcon
Queensland Health

Generated: April 21, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 083729

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NDA 083729 describes IMIPRAMINE HYDROCHLORIDE, which is a drug marketed by Novartis, Leading Pharma Llc, Lederle, Lupin Ltd, Oxford Pharms, Par Pharm, Roxane, Sandoz, Specgx Llc, Sun Pharm Industries, Teva, Usl Pharma, Vangard, Watson Labs, and West Ward, and is included in thirty-six NDAs. It is available from fifteen suppliers. Additional details are available on the IMIPRAMINE HYDROCHLORIDE profile page.

The generic ingredient in IMIPRAMINE HYDROCHLORIDE is imipramine hydrochloride. There are thirty-four drug master file entries for this compound. Fifteen suppliers are listed for this compound. Additional details are available on the imipramine hydrochloride profile page.
Summary for 083729
Tradename:IMIPRAMINE HYDROCHLORIDE
Applicant:Teva
Ingredient:imipramine hydrochloride
Patents:0
Therapeutic Class:Antidepressants
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength10MG
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:No

Profile for product number 003

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength50MG
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:No

Profile for product number 004

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength25MG
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

UBS
Deloitte
Cerilliant
Fish and Richardson
Chubb
Cipla
Julphar
Citi
Queensland Health

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