FDA.reportPublic FDA data

levonorgestrel 52 MG, 8 Year Intrauterine System

RxCUI
1605252
RxNorm name
levonorgestrel 52 MG, 8 Year Intrauterine System
Display name
levonorgestrel 52 MG, 8 Year Intrauterine System
Full name
levonorgestrel 52 MG, 8 Year Intrauterine System
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:14

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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LILETTALEVONORGESTRELAllergan, Inc.aaf0eb2a-f88a-4f26-a445-0fd30176c3262023-06-29Warnings, Adverse reactionsExact identifier
rxcui: 1605252

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
aaf0eb2a-f88a-4f26-a445-0fd30176c326levonorgestrel 52 MG, 8 Year Intrauterine System [PSN] · levonorgestrel 0.000813 MG/HR Intrauterine System [SCD] · levonorgestrel 52 MG, 8 Year Intrauterine System [SY]322These highlights do not include all the information needed to use LILETTA ® safely and effectively. See full prescribing information for LILETTA . LILETTA (levonorgestrel-releasing intrauterine system) Initial U.S. Approval: 1968 (norgestrel)20230629