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Generated: March 19, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 070744

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NDA 070744 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-eight 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 070744
Applicant:Watson Labs
Ingredient:haloperidol lactate
Therapeutic Class:Antipsychotics
Formulation / Manufacturing:see details

Profile for product number 001

Approval Date:May 17, 1988TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Queensland Health
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Boehringer Ingelheim
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