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Serving hundreds of leading biopharmaceutical companies globally:

Julphar
Moodys
Express Scripts
QuintilesIMS
US Army
Farmers Insurance
Fish and Richardson
Queensland Health
Federal Trade Commission

Generated: April 26, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 070726

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NDA 070726 describes HALOPERIDOL, which is a drug marketed by Alpharma, Morton Grove, Pharm Assoc, SCS, Silarx, Teva, Teva Pharms, Abraxis Pharm, Akorn, Baxter Hlthcare Corp, Fosun Pharma, Fresenius Kabi Usa, Gland Pharma Ltd, Marsam Pharms Llc, Mylan Labs Ltd, Sagent Pharms, Smith And Nephew, Solopak, Teva Pharms Usa, Watson Labs, West-ward Pharms Int, Anda Repository, Cycle Pharms Ltd, Duramed Pharms Barr, Lederle, Mylan, Par Pharm, Purepac Pharm, Quantum Pharmics, Royce Labs, Sandoz, Vintage, Zydus Pharms Usa, Hospira, Sandoz Inc, and Actavis Mid Atlantic, and is included in one hundred and six NDAs. It is available from thirty-six suppliers. Additional details are available on the HALOPERIDOL profile page.

The generic ingredient in HALOPERIDOL is haloperidol decanoate. There are twenty drug master file entries for this compound. Eight suppliers are listed for this compound. Additional details are available on the haloperidol decanoate profile page.
Summary for 070726
Tradename:HALOPERIDOL
Applicant:Scs
Ingredient:haloperidol lactate
Patents:0
Therapeutic Class:Antipsychotics
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:CONCENTRATE;ORALStrengthEQ 2MG BASE/ML
Approval Date:Jun 10, 1986TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Moodys
US Department of Justice
Dow
Julphar
McKinsey
Accenture
UBS
Express Scripts
AstraZeneca

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