Ibrutinib

Manufacturer: AX Pharmaceutical Corp
Effective date: 2026-10-08
Label type: BULK INGREDIENT - ANIMAL DRUG
Version: 1
Source: daily-update
Hydrated at: 2026-10-13 04:06:14

Label at a glance#

ProductIbrutinib

Active ingredientIbrutinib

Label structure1 sections

Label contents#

Full prescribing information#

Ibrutinib

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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

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

Ibrutinib

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73377-373	73377-373-01

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
Name	UNII	Kind
Ibrutinib	1X70OSD4VX	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Imbruvica	IBRUTINIB	Pharmacyclics LLC	0dfd0279-ff17-4ea9-89be-9803c71bab44	2025-10-21	Warnings, Adverse reactions	Name fallback generic name: IBRUTINIB

Reported adverse events (FAERS/openFDA)#

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