Generated: November 25, 2017
DrugPatentWatch Database Preview
Details for New Drug Application (NDA): 071187
, which is a drug marketed by Solopak, Smith And Nephew, Sandoz, Morton Grove, Anda Repository, Watson Labs, Teva, Marsam Pharms Llc, Duramed Pharms Barr, Teva Pharms, Alpharma, SCS, Royce Labs, Lederle, Baxter Hlthcare Corp, Cycle Pharms Ltd, Par Pharm, Teva Pharms Usa, Vintage, Pharm Assoc, Sagent Pharms, Mylan Labs Ltd, Akorn, Quantum Pharmics, West-ward Pharms Int, Silarx, Sandoz Inc, Purepac Pharm, Gland Pharma Ltd, Mylan, Zydus Pharms Usa, Abraxis Pharm, Fresenius Kabi Usa, Hospira, and Actavis Mid Atlantic, and is included in one hundred and six NDAs. It is available from thirty-seven 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. Nine suppliers are listed for this compound. Additional details are available on the haloperidol decanoate profile page.
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Summary for product number 001
|Active Rx/OTC/Discontinued:||DISCN||Dosage:||INJECTABLE;INJECTION||Strength||EQ 5MG BASE/ML|
|Approval Date:||Jan 20, 1987||TE:||RLD:||No|
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