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Serving leading biopharmaceutical companies globally:

Accenture
US Department of Justice
Baxter
Harvard Business School
Colorcon
Medtronic
Johnson and Johnson
Moodys
Covington
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Generated: January 17, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 075089

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NDA 075089 describes TICLOPIDINE HYDROCHLORIDE, which is a drug marketed by Actavis Elizabeth, Apotex, Mylan, Sandoz, Sun Pharm Inds Inc, Teva, and Watson Labs, and is included in nine NDAs. It is available from three 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. Three suppliers are listed for this compound. Additional details are available on the ticlopidine hydrochloride profile page.
Summary for 075089
Tradename:TICLOPIDINE HYDROCHLORIDE
Applicant:Apotex
Ingredient:ticlopidine hydrochloride
Patents:0
Therapeutic Class:Blood Products/Modifiers/ Volume Expanders
Formulation / Manufacturing:see details
Pharmacology for NDA: 075089
Physiological EffectDecreased Platelet Aggregation
Suppliers and Packaging for NDA: 075089
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
TICLOPIDINE HYDROCHLORIDE ticlopidine hydrochloride TABLET;ORAL 075089 ANDA Apotex Corp. 60505-0027 60505-0027-4 60 TABLET, FILM COATED in 1 BOTTLE (60505-0027-4)
TICLOPIDINE HYDROCHLORIDE ticlopidine hydrochloride TABLET;ORAL 075089 ANDA Apotex Corp. 60505-0027 60505-0027-2 30 TABLET, FILM COATED in 1 BOTTLE (60505-0027-2)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:TABLET;ORALStrength250MG
Approval Date:Jul 1, 1999TE:ABRLD:No

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Serving leading biopharmaceutical companies globally:

McKinsey
Medtronic
Express Scripts
Dow
Johnson and Johnson
McKesson
Fuji
AstraZeneca
Moodys

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