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Federal Trade Commission
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Generated: April 22, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 075161

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NDA 075161 describes TICLOPIDINE HYDROCHLORIDE, which is a drug marketed by Actavis Elizabeth, Apotex, Mylan, Sun Pharm Inds Inc, Teva, Watson Labs, and Yaopharma Co Ltd, and is included in nine NDAs. It is available from two suppliers. Additional details are available on the TICLOPIDINE HYDROCHLORIDE profile page.

The generic ingredient in TICLOPIDINE HYDROCHLORIDE is ticlopidine hydrochloride. There are nine drug master file entries for this compound. Two suppliers are listed for this compound. Additional details are available on the ticlopidine hydrochloride profile page.
Summary for 075161
Tradename:TICLOPIDINE HYDROCHLORIDE
Applicant:Mylan
Ingredient:ticlopidine hydrochloride
Patents:0
Therapeutic Class:Blood Products/Modifiers/ Volume Expanders
Formulation / Manufacturing:see details

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:TABLET;ORALStrength250MG
Approval Date:Sep 13, 1999TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

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