APPLICATION
ANDA075253
TYPE
ANDA
ORIGINAL APPROVAL
1999-08-20
LATEST ACTION
2002-11-05
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued
Products
TICLOPIDINE HYDROCHLORIDEDiscontinued
TICLOPIDINE HYDROCHLORIDE 250MG · TABLET · ORAL
Approval history
2002-11-05Manufacturing (CMC) · Supplement 7AP
2002-02-15Labeling · Supplement 6AP
2001-11-13Manufacturing (CMC) · Supplement 5AP
2001-11-02Manufacturing (CMC) · Supplement 4AP
2001-02-20Manufacturing (CMC) · Supplement 3AP
2001-01-17Labeling · Supplement 2AP
2000-11-09Manufacturing (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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