Home Applications 079191 Application 079191
Type ANDA
Sponsor TORRENT PHARMS LLC Application Products# Product, Drug, Ingredient table Product Drug Ingredient Form Strength Reference drug Reference standard 001 CETIRIZINE HYDROCHLORIDE ALLERGY CETIRIZINE HYDROCHLORIDE TABLET;ORAL 5MG No No 002 CETIRIZINE HYDROCHLORIDE HIVES RELIEF CETIRIZINE HYDROCHLORIDE TABLET;ORAL 10MG No No 003 CETIRIZINE HYDROCHLORIDE HIVES RELIEF CETIRIZINE HYDROCHLORIDE TABLET;ORAL 5MG No No 004 CETIRIZINE HYDROCHLORIDE ALLERGY CETIRIZINE HYDROCHLORIDE TABLET;ORAL 10MG No No
Source provenance: Browse the complete Orange Book source catalog · source snapshot 44 .
Orange Book products# Current product rows page 1 of 1 · 4 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date A079191-001 CETIRIZINE HYDROCHLORIDE ALLERGY CETIRIZINE HYDROCHLORIDE 5MG TABLET / ORAL 2010-04-15 A079191-002 CETIRIZINE HYDROCHLORIDE HIVES RELIEF CETIRIZINE HYDROCHLORIDE 10MG TABLET / ORAL 2010-04-15 A079191-003 CETIRIZINE HYDROCHLORIDE HIVES RELIEF CETIRIZINE HYDROCHLORIDE 5MG TABLET / ORAL 2010-04-15 A079191-004 CETIRIZINE HYDROCHLORIDE ALLERGY CETIRIZINE HYDROCHLORIDE 10MG TABLET / ORAL 2010-04-15
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 5 of 5 · 176 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 A079191-001 CETIRIZINE HYDROCHLORIDE ALLERGY 5MG TABLET / ORAL 2010-04-15 f41ea6bd6efb…2022-10-28 04:53 UTC 2022-10 A079191-002 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 10MG TABLET / ORAL 2010-04-15 f41ea6bd6efb…2022-10-28 04:53 UTC 2022-10 A079191-003 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 5MG TABLET / ORAL 2010-04-15 f41ea6bd6efb…2022-10-28 04:53 UTC 2022-10 A079191-004 CETIRIZINE HYDROCHLORIDE ALLERGY 10MG TABLET / ORAL 2010-04-15 f41ea6bd6efb…2022-09-29 23:25 UTC 2022-09 A079191-001 CETIRIZINE HYDROCHLORIDE ALLERGY 5MG TABLET / ORAL 2010-04-15 e64feba35796…2022-09-29 23:25 UTC 2022-09 A079191-002 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 10MG TABLET / ORAL 2010-04-15 e64feba35796…2022-09-29 23:25 UTC 2022-09 A079191-003 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 5MG TABLET / ORAL 2010-04-15 e64feba35796…2022-09-29 23:25 UTC 2022-09 A079191-004 CETIRIZINE HYDROCHLORIDE ALLERGY 10MG TABLET / ORAL 2010-04-15 e64feba35796…2022-07-09 03:26 UTC · 3 captures of this ZIP 2022-07 A079191-001 CETIRIZINE HYDROCHLORIDE ALLERGY 5MG TABLET / ORAL 2010-04-15 cb3db0bc1861…2022-07-09 03:26 UTC · 3 captures of this ZIP 2022-07 A079191-002 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 10MG TABLET / ORAL 2010-04-15 cb3db0bc1861…2022-07-09 03:26 UTC · 3 captures of this ZIP 2022-07 A079191-003 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 5MG TABLET / ORAL 2010-04-15 cb3db0bc1861…2022-07-09 03:26 UTC · 3 captures of this ZIP 2022-07 A079191-004 CETIRIZINE HYDROCHLORIDE ALLERGY 10MG TABLET / ORAL 2010-04-15 cb3db0bc1861…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A079191-001 CETIRIZINE HYDROCHLORIDE ALLERGY 5MG TABLET / ORAL 2010-04-15 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A079191-002 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 10MG TABLET / ORAL 2010-04-15 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A079191-003 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 5MG TABLET / ORAL 2010-04-15 a50c72e98297…2026-07-26 02:55 UTC · 3 captures of this ZIP 2026-06 A079191-004 CETIRIZINE HYDROCHLORIDE ALLERGY 10MG TABLET / ORAL 2010-04-15 a50c72e98297…
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 13 · 256 matching rows.
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 · 4 matching rows.
NDC, Name, Nonproprietary name table NDC Name Nonproprietary name Labeler Marketing category Status 13668-030 CETIRIZINE HYDROCHLORIDE CETIRIZINE HYDROCHLORIDE Torrent Pharmaceuticals Limited ANDA Current 13668-030 CETIRIZINE HYDROCHLORIDE CETIRIZINE HYDROCHLORIDE Torrent Pharmaceuticals Limited ANDA Current 13668-590 Cetirizine Hydrochloride Cetirizine Hydrochloride Torrent Pharmaceuticals Limited ANDA Current 13668-590 Cetirizine Hydrochloride Cetirizine Hydrochloride Torrent Pharmaceuticals Limited ANDA Current
Documents# Document, Submission type, Date table Document Submission type Date 9234 ORIG 2010-04-19