FDA.reportPublic FDA data

Nikki 28 Day Pack

RxCUI
1543553
RxNorm name
Nikki 28 Day Pack
Display name
Nikki 28 Day Pack
Full name
Nikki 28 Day Pack
Term type
PSN
Status
DailyMed mapping
Updated
2026-06-04 23:39:10

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
NikkiDROSPIRENONE AND ETHINYL ESTRADIOLLupin Pharmaceuticals, Inc.9aff6034-044c-466d-bf52-18a998d47f662025-12-08Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 1543553

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
9aff6034-044c-466d-bf52-18a998d47f66{24 (drospirenone 3 MG / ethinyl estradiol 0.02 MG Oral Tablet) / 4 (inert ingredients 1 MG Oral Tablet) } Pack [Nikki 28 Day] [BPCK] · Nikki 28 Day Pack [PSN] · Nikki 28 Day Pack [SY]38These highlights do not include all the information needed to use NIKKI safely and effectively. See full prescribing information for NIKKI. NIKKI TM (Drospirenone / ethinyl estradiol) tablets, for oral use Initial U.S. Approval: 200120251208