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Nilotinib

NILOTINIB HYDROCHLORIDE MONOHYDRATE

Active ingredient 2 prescription 6 with labelling

Overview

Source: NDC Directory

Ingredient name

NILOTINIB HYDROCHLORIDE MONOHYDRATE

Base moiety

NILOTINIB

RxNorm CUI

746606

UNII

5JHU0N1R6K

Medication products

Brand names

Dosage forms

FAERS reports

29,318 · not a risk measure

Products containing this ingredient

Source: NDC Directory 7 products

Nilotinib Powder
3 NDC
Nilotinib Hydrochloride Powder
3 NDC
Nilotinib Hydrochloride (Monohydrate) Powder
1 NDC
Nilotinib Hydrochloride Monohydrate Powder
6 NDC
Nilotinib Premix Powder
1 NDC
nilotinib Capsule
Rx ANDA TE AB 2 recalls 21 NDC
Tasigna nilotinib · Capsule
Rx NDA TE AB 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	5	Nilotinib, Nilotinib Hydrochloride, Nilotinib Hydrochloride (Monohydrate), Nilotinib Hydrochloride Monohydrate …
Capsule	2	nilotinib, Tasigna

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