Ondansetron — ingredient monograph

Overview

Source: NDC Directory

Ingredient name

ONDANSETRON

Base moiety

ONDANSETRON

RxNorm CUI

283504

UNII

4AF302ESOS

Medication products

7

Brand names

1

Dosage forms

4

FAERS reports

121,842 · not a risk measure

Products containing this ingredient

Source: NDC Directory 7 products

Ondansetron Powder
9 NDC
ONDANSETRON BASE Ondansetron Base · Powder
1 NDC
Ondansetron Hydrochloride Powder
23 NDC
ondansetron oral Film
1 NDC
ondansetron oral film Film
1 NDC
Ondansetron Injection
Rx ANDA TE AP 2 recalls 33 NDC
Ondansetron Tablet, Orally Disintegrating
Rx ANDA TE AB 98 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	3	Ondansetron, ONDANSETRON BASE, Ondansetron Hydrochloride
Film	2	ondansetron oral, ondansetron oral film
Injection	1	Ondansetron
TABLET, Orally Disintegrating	1	Ondansetron

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