FDA.reportPublic FDA data

cetirizine hydrochloride 10 MG in 1 ML Injection

RxCUI
2261746
RxNorm name
cetirizine hydrochloride 10 MG in 1 ML Injection
Display name
cetirizine hydrochloride 10 MG in 1 ML Injection
Full name
cetirizine hydrochloride 10 MG in 1 ML Injection
Term type
PSN
Status
DailyMed mapping
Updated
2026-06-04 23:39:27

RxNav Current And Historical NDCs#

RxNav current and historical NDC rows page 1 of 1 · 0 matching rows.

No records found.

UNII Substances#

UNII substance links page 1 of 1 · 0 matching rows.

No records found.

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
QUZYTTIRCETIRIZINE HYDROCHLORIDEESTEVE PHARMACEUTICALS, S.A.573770f6-b76e-f6ba-e063-6294a90aa54d2026-08-13Warnings, Adverse reactionsExact identifier
rxcui: 2261746
QUZYTTIRCETIRIZINE HYDROCHLORIDETerSera Therapeutics LLCf33e859d-ebc9-4d4f-a57d-204c48760d202026-03-04Warnings, Adverse reactionsExact identifier
rxcui: 2261746

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

DailyMed RxNorm Mappings#

unique DailyMed labels mapped to this RxNorm concept page 1 of 1 · 1 matching rows.

Set ID, RxNorm mappings, Terms table
Set IDRxNorm mappingsTermsSPL versionLabelEffective
f33e859d-ebc9-4d4f-a57d-204c48760d20cetirizine hydrochloride 10 MG in 1 ML Injection [PSN] · 1 ML cetirizine hydrochloride 10 MG/ML Injection [SCD] · cetirizine hydrochloride 10 MG per 1 ML Injection [SY]38These highlights do not include all the information needed to use QUZYTTIR ® safely and effectively. See full prescribing information for QUZYTTIR ® . QUZYTTIR ® (cetirizine hydrochloride injection), for intravenous use Initial U.S. Approval: 199520260304