FDA.reportPublic FDA data

Iclevia 91 Day Pack

RxCUI
2049264
RxNorm name
Iclevia 91 Day Pack
Display name
Iclevia 91 Day Pack
Full name
Iclevia 91 Day Pack
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:38:45

RxNav Current And Historical NDCs#

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

No records found.

UNII Substances#

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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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
IcleviaLEVONORGESTREL AND ETHINYL ESTRADIOLAurobindo Pharma Limited00657f4e-9df8-4f58-91a0-eff5a467f9882024-07-02Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 2049264

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
00657f4e-9df8-4f58-91a0-eff5a467f988{84 (ethinyl estradiol 0.03 MG / levonorgestrel 0.15 MG Oral Tablet) / 7 (inert ingredients 1 MG Oral Tablet) } Pack [Iclevia 91 Day] [BPCK] · Iclevia 91 Day Pack [PSN] · Iclevia 91 Day Pack [SY]39These highlights do not include all the information needed to use ICLEVIA safely and effectively. See full prescribing information for ICLEVIA. ICLEVIA (levonorgestrel and ethinyl estradiol tablets) for oral use Initial U.S. Approval: 198220240702