FDA.reportPublic FDA data

Abigale Lo 0.5/0.1 28 Day Pack

RxCUI
2706647
RxNorm name
Abigale Lo 0.5/0.1 28 Day Pack
Display name
Abigale Lo 0.5/0.1 28 Day Pack
Full name
Abigale Lo 0.5/0.1 28 Day Pack
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:24

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
ABIGALE LOESTRADIOL AND NORETHINDRONE ACETATEXiromed LLCdf013d36-de10-0607-7e12-95ed43bf7ee92024-09-17Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 2706647

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
df013d36-de10-0607-7e12-95ed43bf7ee9{28 (estradiol 0.5 MG / norethindrone acetate 0.1 MG Oral Tablet) } Pack [Abigale Lo 0.5/0.1 28 Day] [BPCK] · Abigale Lo 0.5/0.1 28 Day Pack [PSN] · Abigale Lo 0.5/0.1 28 Day Pack [SY]31These highlights do not include all the information needed to use ABIGALE and ABIGALE LO safely and effectively. See full prescribing information for ABIGALE and ABIGALE LO . ABIGALE TM and ABIGALE TM LO (estradiol/norethindrone acetate) tablets, for oral use Initial U.S. Approval: 199820240917