APPLICATION
ANDA075161
TYPE
ANDA
ORIGINAL APPROVAL
1999-09-13
LATEST ACTION
2002-10-29
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued
Products
TICLOPIDINE HYDROCHLORIDEDiscontinued
TICLOPIDINE HYDROCHLORIDE 250MG · TABLET · ORAL
Approval history
2002-10-29Labeling · Supplement 5AP
2002-03-13Labeling · Supplement 4AP
2001-05-30Manufacturing (CMC) · Supplement 3AP
2001-01-03Labeling · Supplement 2AP
2000-11-06Manufacturing (CMC) · Supplement 1AP
Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.
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