Oriahnn 28 Day Kit

RxCUI: 2371768
RxNorm name: Oriahnn 28 Day Kit
Display name: Oriahnn 28 Day Kit
Full name: Oriahnn 28 Day Kit
Term type: PSN
Status: DailyMed mapping
Updated: 2026-06-04 23:39:10

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.

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Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Oriahnn	ELAGOLIX AND ESTRADIOL AND NORETHISTERONE	AbbVie Inc.	99f6eee7-7e52-6999-7eb8-488d06dd1710	2025-12-19	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 2371768

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set ID	RxNorm string	TTY	SPL version	Label	Effective
99f6eee7-7e52-6999-7eb8-488d06dd1710	Oriahnn 28 Day Kit	PSN	41	These highlights do not include all the information needed to use ORIAHNN safely and effectively. See full prescribing information for ORIAHNN. ORIAHNN ® (elagolix, estradiol, and norethindrone acetate capsules; elagolix capsules), co-packaged for oral use Initial U.S. Approval: 2020	20251219
99f6eee7-7e52-6999-7eb8-488d06dd1710	Oriahnn 28 Day Kit	SY	41	These highlights do not include all the information needed to use ORIAHNN safely and effectively. See full prescribing information for ORIAHNN. ORIAHNN ® (elagolix, estradiol, and norethindrone acetate capsules; elagolix capsules), co-packaged for oral use Initial U.S. Approval: 2020	20251219
99f6eee7-7e52-6999-7eb8-488d06dd1710	{28 (elagolix 300 MG / estradiol 1 MG / norethindrone 0.5 MG Oral Capsule) / 28 (elagolix 300 MG Oral Capsule) } Pack [Oriahnn 28 Day Kit]	BPCK	41	These highlights do not include all the information needed to use ORIAHNN safely and effectively. See full prescribing information for ORIAHNN. ORIAHNN ® (elagolix, estradiol, and norethindrone acetate capsules; elagolix capsules), co-packaged for oral use Initial U.S. Approval: 2020	20251219