Risperidone — ingredient monograph

Overview

Source: NDC Directory

Ingredient name

RISPERIDONE

Base moiety

RISPERIDONE

RxNorm CUI

312832

UNII

L6UH7ZF8HC

Medication products

12

Brand names

4

Dosage forms

8

FAERS reports

131,094 · not a risk measure

Products containing this ingredient

Source: NDC Directory 12 products

RISPERDAL Risperdal · Powder
1 NDC
RISPERDAL risperidone · Solution
Rx NDA TE AA 1 NDC
risperidone Injection, Suspension
4 NDC
Risperidone Powder
18 NDC
Risperidone Injection, Powder, for Solution
2 NDC
RISPERDAL risperidone · Tablet
Rx NDA TE AB 5 NDC
RISPERDAL M-TAB risperidone · Tablet, Orally Disintegrating
Rx NDA 5 NDC
Risperidone Tablet
Rx ANDA TE AB 75 NDC
Risperidone Tablet, Film Coated
Rx ANDA TE AB 45 NDC
Risperidone Solution
Rx ANDA TE AA 12 NDC
Risperidone Tablet, Orally Disintegrating
Rx ANDA TE AB 32 NDC
UZEDY risperidone · Injection, Suspension, Extended Release
Rx NDA 7 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	2	RISPERDAL, Risperidone
Solution	2	RISPERDAL, Risperidone
Tablet	2	RISPERDAL, Risperidone
TABLET, Orally Disintegrating	2	RISPERDAL M-TAB, Risperidone
INJECTION, Suspension	1	risperidone
INJECTION, POWDER, For Solution	1	Risperidone
TABLET, Film Coated	1	Risperidone
INJECTION, SUSPENSION, Extended Release	1	UZEDY

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