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Serving hundreds of leading biopharmaceutical companies globally:

McKinsey
Mallinckrodt
Express Scripts
Harvard Business School
McKesson
Cerilliant
Dow
Argus Health
Federal Trade Commission

Generated: April 26, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 072353

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NDA 072353 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 072353
Tradename:HALOPERIDOL
Applicant:Watson Labs
Ingredient:haloperidol
Patents:0
Formulation / Manufacturing:see details
Medical Subject Heading (MeSH) Categories for 072353

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength20MG
Approval Date:Aug 27, 1991TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Mallinckrodt
Medtronic
Harvard Business School
McKesson
Fish and Richardson
Accenture
Teva
McKinsey
Dow

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