FDA.reportPublic FDA data

X

Manufacturer
AX Pharmaceutical Corp
Effective date
2017-04-11
Label type
BULK INGREDIENT
Version
1
Source
full-release
Hydrated at
2026-06-01 02:48:26

Label at a glance#

ProductX
Active ingredientRUXOLITINIB PHOSPHATE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
54477ffc-bf5d-4583-bcf6-d041bdba36f1Product name120220316
95a946d8-a784-4eb7-bff4-2194e4331c6fProduct name120190828

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62157-406-01X5 g in 1 JARPOWDER51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62157-406X (RUXOLITINIB PHOSPHATE) POWDER [AX PHARMACEUTICAL CORP]11 package rows20170411_db04a102-c4a3-4a8b-811f-00750fdbda43.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62157-40662157-406-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
RUXOLITINIB PHOSPHATE436LRU32H5ACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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