Ondansetron — ingredient monograph

Overview

Source: NDC Directory

Ingredient name

ONDANSETRON HYDROCHLORIDE

Base moiety

ONDANSETRON

RxNorm CUI

1740467

UNII

NMH84OZK2B

Medication products

15

Brand names

4

Dosage forms

6

FAERS reports

121,842 · not a risk measure

Products containing this ingredient

Source: NDC Directory 15 products

Ondansetron Powder
9 NDC
Ondansetron HCl Powder
1 NDC
Ondansetron HCl Dihydrate Powder
1 NDC
ONDANSETRON HYDROCH LORIDE Ondansetron Hydroch Loride · Powder
1 NDC
Ondansetron Hydrochloride Powder
23 NDC
Ondansetron Hydrochloride Dihydrate Powder
1 NDC
Ondansetron Injection
Rx ANDA TE AP 2 recalls 33 NDC
Ondansetron Solution
Rx ANDA TE AA 10 NDC
Ondansetron Tablet, Film Coated
Rx ANDA TE AB 1 recall 30 NDC
Ondansetron Tablet
Rx ANDA TE AB 7 NDC
ONDANSETRON Ondansetron · Injection, Solution
Rx ANDA TE AP 2 recalls 14 NDC
Ondansetron HCL Tablet, Film Coated
Rx ANDA TE AB 3 NDC
Ondansetron Hydrochloride Tablet, Film Coated
Rx ANDA TE AB 1 recall 71 NDC
Ondansetron Hydrochloride Solution
Rx ANDA TE AA 1 recall 6 NDC
ondansetron hydrochloride Injection
Rx ANDA 2 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	6	Ondansetron, Ondansetron HCl, Ondansetron HCl Dihydrate, ONDANSETRON HYDROCH LORIDE …
TABLET, Film Coated	3	Ondansetron, Ondansetron HCL, Ondansetron Hydrochloride
Injection	2	Ondansetron, ondansetron hydrochloride
Solution	2	Ondansetron, Ondansetron Hydrochloride
Tablet	1	Ondansetron
INJECTION, Solution	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