Kisqali 600 MG Daily Dose Carton Pack

RxCUI
1873995
RxNorm name
Kisqali 600 MG Daily Dose Carton Pack
Display name
Kisqali 600 MG Daily Dose Carton Pack
Full name
Kisqali 600 MG Daily Dose Carton Pack
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:14

RxNav Current And Historical NDCs#

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

No records found.

UNII Substances#

UNII substance links page 1 of 1 · 0 matching rows.

No records found.

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
KISQALIRIBOCICLIBNovartis Pharmaceuticals Corporationaaeaef94-f3f5-4367-8ea2-b181d7be2da82026-07-01Warnings, Adverse reactionsExact identifier
rxcui: 1873995

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set IDRxNorm stringTTYSPL versionLabelEffective
aaeaef94-f3f5-4367-8ea2-b181d7be2da8Kisqali 600 MG Daily Dose Carton PackSY27These 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: 201720251215
aaeaef94-f3f5-4367-8ea2-b181d7be2da8{63 (ribociclib 200 MG Oral Tablet [Kisqali]) } Pack [Kisqali 600 MG Daily Dose Carton]BPCK27These 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: 201720251215
aaeaef94-f3f5-4367-8ea2-b181d7be2da8Kisqali 600 MG Daily Dose Carton PackPSN27These 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: 201720251215