Home Applications 075326 Application 075326
Type ANDA
Sponsor YAOPHARMA CO LTD Application Products# Product, Drug, Ingredient table Product Drug Ingredient Form Strength Reference drug Reference standard 001 TICLOPIDINE HYDROCHLORIDE TICLOPIDINE HYDROCHLORIDE TABLET;ORAL 250MG No No
Source provenance: Browse the complete Orange Book source catalog · source snapshot 44 .
Orange Book products# Current product rows page 1 of 1 · 1 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A075326-001 TICLOPIDINE HYDROCHLORIDE TICLOPIDINE HYDROCHLORIDE 250MG TABLET / ORAL 1999-08-20
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Product history page 2 of 2 · 44 observed states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2022-10-28 04:53 UTC 2022-10 A075326-001 TICLOPIDINE HYDROCHLORIDE 250MG TABLET / ORAL 1999-08-20 f41ea6bd6efb…2022-09-29 23:25 UTC 2022-09 A075326-001 TICLOPIDINE HYDROCHLORIDE 250MG TABLET / ORAL 1999-08-20 e64feba35796…2022-07-09 03:26 UTC · 3 captures of this ZIP 2022-07 A075326-001 TICLOPIDINE HYDROCHLORIDE 250MG TABLET / ORAL 1999-08-20 cb3db0bc1861…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A075326-001 TICLOPIDINE HYDROCHLORIDE 250MG TABLET / ORAL 1999-08-20 a50c72e98297…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
NDC Listings For This Application# NDC listings for this application page 1 of 1 · 1 matching rows.
NDC, Name, Nonproprietary name table NDC Name Nonproprietary name Labeler Marketing category Status 0185-0115 Ticlopidine Hydrochloride Ticlopidine Hydrochloride Eon Labs, Inc. ANDA Current
Documents# Document, Submission type, Date table Document Submission type Date 39479 ORIG 2004-06-18 22459 ORIG 2001-12-20 8620 ORIG 1999-08-20