tolvaptan 30 MG Oral Tablet

RxCUI: 2719337
RxNorm name: tolvaptan 30 MG Oral Tablet
Display name: tolvaptan 30 MG Oral Tablet
Full name: tolvaptan 30 MG Oral Tablet
Term type: PSN
Status: DailyMed mapping
Updated: 2026-06-04 23:38:55

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 · 3 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Tolvaptan	TOLVAPTAN	Ascend Laboratories, LLC	82ef58ef-ce46-434e-bf99-89fce51094f1	2026-08-20	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 2719337
Jynarque	TOLVAPTAN	Otsuka America Pharmaceutical, Inc.	3febc0a1-9e5a-4ce0-843d-210f21d862c4	2025-11-06	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 2719337
TOLVAPTAN	TOLVAPTAN	Lupin Pharmaceuticals, Inc.	9ba38e23-ca66-4406-92af-bbb8fad00e16	2025-05-09	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 2719337

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
3febc0a1-9e5a-4ce0-843d-210f21d862c4	tolvaptan 30 MG Oral Tablet [PSN] · tolvaptan 30 MG Oral Tablet [SCD]	2	19	These highlights do not include all the information needed to use JYNARQUE safely and effectively. See full prescribing information for JYNARQUE. JYNARQUE ® (tolvaptan) tablets, for oral use Initial U.S. Approval: 2009	20251106
9ba38e23-ca66-4406-92af-bbb8fad00e16	tolvaptan 30 MG Oral Tablet [PSN] · tolvaptan 30 MG Oral Tablet [SCD]	2	6	These highlights do not include all the information needed to use TOLVAPTAN TABLETS safely and effectively. See full prescribing information for TOLVAPTAN TABLETS. TOLVAPTAN tablets for oral use Initial U.S. Approval: 2009	20250509