FDA.reportPublic FDA data

Blisovi 24 Fe 1/20 28 Day Pack

RxCUI
1722680
RxNorm name
Blisovi 24 Fe 1/20 28 Day Pack
Display name
Blisovi 24 Fe 1/20 28 Day Pack
Full name
Blisovi 24 Fe 1/20 28 Day Pack
Term type
PSN
Status
DailyMed mapping
Updated
2026-06-04 23:38:48

RxNav Current And Historical NDCs#

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UNII Substances#

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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
Blisovi 24 FeNORETHINDRONE ACETATE AND ETHINYL ESTRADIOLLupin Pharmaceuticals, Inc.1183b048-16f3-47a4-a42f-22ba07b2bb522025-11-18Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 1722680

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
1183b048-16f3-47a4-a42f-22ba07b2bb52{24 (ethinyl estradiol 0.02 MG / norethindrone acetate 1 MG Oral Tablet) / 4 (ferrous fumarate 75 MG Oral Tablet) } Pack [Blisovi 24 Fe 1/20 28 Day] [BPCK] · Blisovi 24 Fe 1/20 28 Day Pack [PSN] · Blisovi 24 Fe 1/20 28 Day Pack [SY]38These highlights do not include all the information needed to use BLISOVI 24 Fe safely and effectively. See Full Prescribing Information for BLISOVI 24 Fe. Blisovi TM 24 Fe [norethindrone acetate and ethinyl estradiol tablets USP, (1 mg/0.02 mg) and ferrous fumarate tablets, (75 mg)] for Oral Use Initial U.S. Approval: 196820251118