Cardura 2 MG Oral Tablet

RxCUI: 104368
RxNorm name: Cardura 2 MG Oral Tablet
Display name: Cardura 2 MG Oral Tablet
Full name: Cardura 2 MG Oral Tablet
Term type: SY
Status: DailyMed mapping
Updated: 2026-06-04 23:39:27

RxNav Current And Historical NDCs#

RxNav current and historical NDC rows page 1 of 1 · 0 matching rows.

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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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Cardura	DOXAZOSIN	Viatris Specialty LLC	5e1f5e49-2da1-43ab-9795-228a8bcc5a82	2023-10-15	Warnings, Adverse reactions	Exact identifier rxcui: 104368
Cardura	DOXAZOSIN	ROERIG	eefc47bc-c10f-49bb-8ef7-5999f798ab39	2022-01-20	Warnings, Adverse reactions	Exact identifier rxcui: 104368

DailyMed RxNorm Mappings#

unique DailyMed labels mapped to this RxNorm concept page 1 of 1 · 2 matching rows.

Set ID, RxNorm mappings, Terms table
Set ID	RxNorm mappings	Terms	SPL version	Label	Effective
eefc47bc-c10f-49bb-8ef7-5999f798ab39	Cardura 2 MG Oral Tablet [PSN] · doxazosin 2 MG Oral Tablet [Cardura] [SBD] · Cardura (as doxazosin mesylate) 2 MG Oral Tablet [SY] · Cardura 2 MG Oral Tablet [SY]	4	25	These highlights do not include all the information needed to use CARDURA safely and effectively. See full prescribing information for CARDURA. CARDURA ® (doxazosin) tablets, for oral use Initial U.S. Approval: 1990	20220120
5e1f5e49-2da1-43ab-9795-228a8bcc5a82	Cardura 2 MG Oral Tablet [PSN] · doxazosin 2 MG Oral Tablet [Cardura] [SBD] · Cardura (as doxazosin mesylate) 2 MG Oral Tablet [SY] · Cardura 2 MG Oral Tablet [SY]	4	2	These highlights do not include all the information needed to use CARDURA safely and effectively. See full prescribing information for CARDURA . CARDURA ® (doxazosin) tablets, for oral use Initial U.S. Approval: 1990	20231015