Crizotinib

Manufacturer
BLUEBAY SHANDONG CO.,LTD
Effective date
2020-03-09
Label type
BULK INGREDIENT
Version
1
Source
full-release
Hydrated at
2026-06-01 02:49:31

Label at a glance#

ProductCrizotinib
Active ingredientCRIZOTINIB
Label structure1 sections

Label contents#

Full prescribing information#

Crizotinib

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f170fd86-ec78-ad31-9645-3b581b85a0f1Product name220250620

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73309-090-01Crizotinib10 g in 1 JARPOWDER101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73309-090CRIZOTINIB POWDER [BLUEBAY SHANDONG CO.,LTD]11 package rows20200310_893c7747-7aa3-4660-a863-d89ded906ad7.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 1 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73309-09073309-090-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
CRIZOTINIB53AH36668SACTIB

Source Document#

Source XML

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
XalkoriCRIZOTINIBPfizer Laboratories Div Pfizer Inc2a51b0de-47d6-455e-a94c-d2c737b04ff72025-07-22Warnings, Adverse reactionsName fallback
generic name: CRIZOTINIB

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.