Home NDC 58602-861 Cetirizine Hydrochloride (Allergy)
Product NDC 58602-861
11-digit product format 586020861
Labeler code 58602
Product ID 58602-861_20dddc76-5ac2-498d-bff3-2d722a58891e
Type HUMAN OTC DRUG
Nonproprietary name Cetirizine Hydrochloride
Dosage form TABLET
Route ORAL
Labeler Aurohealth LLC
Application ANDA090760
Marketing category ANDA
Marketing start 2023-02-10
Substance CETIRIZINE HYDROCHLORIDE
Active strength 10 mg/1
Pharmacologic classes Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes
Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 36 matching rows.
View current auxiliary records. · View the auxiliary file history.
Source provenance: Browse the complete Orange Book source catalog · source snapshot 43 .
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 A090760-001 CETIRIZINE HYDROCHLORIDE ALLERGY CETIRIZINE HYDROCHLORIDE 5MG TABLET / ORAL 2015-08-05 A090760-002 CETIRIZINE HYDROCHLORIDE HIVES RELIEF CETIRIZINE HYDROCHLORIDE 5MG TABLET / ORAL 2015-08-05 A090760-003 CETIRIZINE HYDROCHLORIDE ALLERGY CETIRIZINE HYDROCHLORIDE 10MG TABLET / ORAL 2015-08-05 A090760-004 CETIRIZINE HYDROCHLORIDE HIVES RELIEF CETIRIZINE HYDROCHLORIDE 10MG TABLET / ORAL 2015-08-05
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 1 of 5 · 172 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 2026-09-14 22:38:34 2026-08 A090760-001 CETIRIZINE HYDROCHLORIDE ALLERGY 5MG TABLET / ORAL 2015-08-05 84e616aacf4f…2026-09-14 22:38:34 2026-08 A090760-002 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 5MG TABLET / ORAL 2015-08-05 84e616aacf4f…2026-09-14 22:38:34 2026-08 A090760-003 CETIRIZINE HYDROCHLORIDE ALLERGY 10MG TABLET / ORAL 2015-08-05 84e616aacf4f…2026-09-14 22:38:34 2026-08 A090760-004 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 10MG TABLET / ORAL 2015-08-05 84e616aacf4f…2026-08-18 06:07:40 2026-07 A090760-001 CETIRIZINE HYDROCHLORIDE ALLERGY 5MG TABLET / ORAL 2015-08-05 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A090760-002 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 5MG TABLET / ORAL 2015-08-05 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A090760-003 CETIRIZINE HYDROCHLORIDE ALLERGY 10MG TABLET / ORAL 2015-08-05 caaa826d4ba7…2026-08-18 06:07:40 2026-07 A090760-004 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 10MG TABLET / ORAL 2015-08-05 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 A090760-001 CETIRIZINE HYDROCHLORIDE ALLERGY 5MG TABLET / ORAL 2015-08-05 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A090760-002 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 5MG TABLET / ORAL 2015-08-05 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A090760-003 CETIRIZINE HYDROCHLORIDE ALLERGY 10MG TABLET / ORAL 2015-08-05 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 A090760-004 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 10MG TABLET / ORAL 2015-08-05 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A090760-001 CETIRIZINE HYDROCHLORIDE ALLERGY 5MG TABLET / ORAL 2015-08-05 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A090760-002 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 5MG TABLET / ORAL 2015-08-05 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A090760-003 CETIRIZINE HYDROCHLORIDE ALLERGY 10MG TABLET / ORAL 2015-08-05 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 A090760-004 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 10MG TABLET / ORAL 2015-08-05 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 A090760-001 CETIRIZINE HYDROCHLORIDE ALLERGY 5MG TABLET / ORAL 2015-08-05 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A090760-002 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 5MG TABLET / ORAL 2015-08-05 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A090760-003 CETIRIZINE HYDROCHLORIDE ALLERGY 10MG TABLET / ORAL 2015-08-05 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 A090760-004 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 10MG TABLET / ORAL 2015-08-05 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A090760-001 CETIRIZINE HYDROCHLORIDE ALLERGY 5MG TABLET / ORAL 2015-08-05 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A090760-002 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 5MG TABLET / ORAL 2015-08-05 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A090760-003 CETIRIZINE HYDROCHLORIDE ALLERGY 10MG TABLET / ORAL 2015-08-05 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 A090760-004 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 10MG TABLET / ORAL 2015-08-05 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A090760-001 CETIRIZINE HYDROCHLORIDE ALLERGY 5MG TABLET / ORAL 2015-08-05 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A090760-002 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 5MG TABLET / ORAL 2015-08-05 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A090760-003 CETIRIZINE HYDROCHLORIDE ALLERGY 10MG TABLET / ORAL 2015-08-05 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 A090760-004 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 10MG TABLET / ORAL 2015-08-05 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A090760-001 CETIRIZINE HYDROCHLORIDE ALLERGY 5MG TABLET / ORAL 2015-08-05 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A090760-002 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 5MG TABLET / ORAL 2015-08-05 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A090760-003 CETIRIZINE HYDROCHLORIDE ALLERGY 10MG TABLET / ORAL 2015-08-05 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 A090760-004 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 10MG TABLET / ORAL 2015-08-05 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A090760-001 CETIRIZINE HYDROCHLORIDE ALLERGY 5MG TABLET / ORAL 2015-08-05 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A090760-002 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 5MG TABLET / ORAL 2015-08-05 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A090760-003 CETIRIZINE HYDROCHLORIDE ALLERGY 10MG TABLET / ORAL 2015-08-05 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 A090760-004 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 10MG TABLET / ORAL 2015-08-05 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A090760-001 CETIRIZINE HYDROCHLORIDE ALLERGY 5MG TABLET / ORAL 2015-08-05 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A090760-002 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 5MG TABLET / ORAL 2015-08-05 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A090760-003 CETIRIZINE HYDROCHLORIDE ALLERGY 10MG TABLET / ORAL 2015-08-05 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 A090760-004 CETIRIZINE HYDROCHLORIDE HIVES RELIEF 10MG TABLET / ORAL 2015-08-05 5bbf6a4d5a75…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Cetirizine Hydrochloride (Allergy)
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CETIRIZINE HYDROCHLORIDE 10 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 64O047KTOA Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1014678 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 1 · 18 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 58602-861-40 58602086140 500 TABLET in 1 BOTTLE (58602-861-40) 500 tablet 2026-05-25 No No Current