Last Updated: September 28, 2026

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, Chartwell Rx, Mylan, Natco Pharma, Sun Pharm Inds Inc, Teva, and Watson Labs, and is included in nine NDAs. Additional details are available on the TICLOPIDINE HYDROCHLORIDE profile page.

The generic ingredient in TICLOPIDINE HYDROCHLORIDE is ticlopidine hydrochloride. There is one drug master file entry 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

Medical Subject Heading (MeSH) Categories for 075161

Cytochrome P-450 CYP2C19 Inhibitors
Fibrinolytic Agents
Platelet Aggregation Inhibitors
Purinergic P2Y Receptor Antagonists

Profile for product number 001

Active Rx/OTC/Discontinued:	DISCN	Dosage:	TABLET;ORAL			Strength	250MG
Approval Date:	Sep 13, 1999	TE:		RLD:	No

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