FDA.reportPublic FDA data

Mimvey 28 Day Pack

RxCUI
1359129
RxNorm name
Mimvey 28 Day Pack
Display name
Mimvey 28 Day Pack
Full name
Mimvey 28 Day Pack
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:16

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
MimveyESTRADIOL AND NORETHINDRONE ACETATETeva Pharmaceuticals USA, Inc.b1c5c06b-9ce2-4bf7-9693-e37608055a142024-05-31Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 1359129

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
b1c5c06b-9ce2-4bf7-9693-e37608055a14{28 (estradiol 1 MG / norethindrone acetate 0.5 MG Oral Tablet) } Pack [Mimvey] [BPCK] · Mimvey 28 Day Pack [PSN] · Mimvey 28 Day Pack [SY]316These highlights do not include all the information needed to use MIMVEY TABLETS safely and effectively. See full prescribing information for MIMVEY TABLETS. MIMVEY ® (estradiol and norethindrone acetate) tablets, for oral use Initial U.S. Approval: 199820240531