ribociclib 600 MG Daily Dose Carton Pack, 3 Blister Cards, 21 Tablets Each

RxCUI: 1873994
RxNorm name: ribociclib 600 MG Daily Dose Carton Pack, 3 Blister Cards, 21 Tablets Each
Display name: ribociclib 600 MG Daily Dose Carton Pack, 3 Blister Cards, 21 Tablets Each
Full name: ribociclib 600 MG Daily Dose Carton Pack, 3 Blister Cards, 21 Tablets Each
Term type: SY
Status: DailyMed mapping
Updated: 2026-06-04 23:39:14

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
KISQALI	RIBOCICLIB	Novartis Pharmaceuticals Corporation	aaeaef94-f3f5-4367-8ea2-b181d7be2da8	2026-07-01	Warnings, Adverse reactions	Exact identifier rxcui: 1873994

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set ID	RxNorm string	TTY	SPL version	Label	Effective
aaeaef94-f3f5-4367-8ea2-b181d7be2da8	ribociclib 600 MG Daily Dose Carton Pack, 3 Blister Cards, 21 Tablets Each	SY	27	These highlights do not include all the information needed to use KISQALI safely and effectively. See full prescribing information for KISQALI. KISQALI ® (ribociclib) tablets, for oral use Initial U.S. Approval: 2017	20251215
aaeaef94-f3f5-4367-8ea2-b181d7be2da8	ribociclib 600 MG Daily Dose, 200 MG Oral Tablet 63 Count Pack	PSN	27	These highlights do not include all the information needed to use KISQALI safely and effectively. See full prescribing information for KISQALI. KISQALI ® (ribociclib) tablets, for oral use Initial U.S. Approval: 2017	20251215
aaeaef94-f3f5-4367-8ea2-b181d7be2da8	{63 (ribociclib 200 MG Oral Tablet) } Pack	GPCK	27	These highlights do not include all the information needed to use KISQALI safely and effectively. See full prescribing information for KISQALI. KISQALI ® (ribociclib) tablets, for oral use Initial U.S. Approval: 2017	20251215