Ibrutinib — ingredient monograph

Overview

Source: NDC Directory

Ingredient name

IBRUTINIB

Base moiety

IBRUTINIB

RxNorm CUI

1442986

UNII

1X70OSD4VX

Medication products

14

Brand names

1

Dosage forms

5

FAERS reports

80,310 · not a risk measure

Products containing this ingredient

Source: NDC Directory 14 products

Ibrutinib Tablet, Film Coated
5 NDC
Ibrutinib Powder
12 NDC
Ibrutinib Capsule
4 NDC
IBRUTINIB Ibrutinib · Tablet
1 NDC
Ibrutinib (Form S4) Powder
1 NDC
Ibrutinib (Form-A) Powder
1 NDC
Ibrutinib (Form-C) Powder
1 NDC
Ibrutinib (Form-M5) Powder
1 NDC
Ibrutinib HFCC Powder
1 NDC
Ibrutinib(Amorphous) Powder
1 NDC
Ibutinib Powder
1 NDC
Imbruvica Ibrutinib · Suspension
Rx NDA 1 NDC
Imbruvica Ibrutinib · Capsule
Rx NDA TE AB 2 NDC
Imbruvica Ibrutinib · Tablet, Film Coated
Rx NDA 3 NDC

Entries without a link are products listed by the FDA that carry no approval record, therapeutic equivalence rating or official labelling, so they have no detail page. Their facts are shown inline.

By dosage form

How this ingredient is presented across the catalogue.
Dosage form	Products	Examples
Powder	8	Ibrutinib, Ibrutinib (Form S4), Ibrutinib (Form-A), Ibrutinib (Form-C) …
TABLET, Film Coated	2	Ibrutinib, Imbruvica
Capsule	2	Ibrutinib, Imbruvica
Tablet	1	IBRUTINIB
Suspension	1	Imbruvica

Sources for this page

Dataset	Agency	Used for
NDC Directory	FDA	Ingredient name, strengths, products, labelers, packages
DailyMed RxNorm mappings	NLM	RxNorm concept identifier (RxCUI)
FAERS	FDA	Adverse event report totals