Fesoterodine — ingredient monograph

Overview

Source: NDC Directory

Ingredient name

FESOTERODINE FUMARATE

Base moiety

FESOTERODINE

RxNorm CUI

810071

UNII

EOS72165S7

Medication products

5

Brand names

3

Dosage forms

3

FAERS reports

10,773 · not a risk measure

Products containing this ingredient

Source: NDC Directory 5 products

Fesoterodine Powder
2 NDC
Fesoterodine Fumarate Powder
5 NDC
FESOTERODINE FUMARATE Fesoterodine Fumarate · Tablet, Film Coated, Extended Release
Rx ANDA TE AB 10 NDC
Fesoterodine Fumarate Tablet, Extended Release
Rx ANDA TE AB 2 recalls 14 NDC
Toviaz fesoterodine fumarate · Tablet, Film Coated, Extended Release
Rx NDA TE AB 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	2	Fesoterodine, Fesoterodine Fumarate
TABLET, Film COATED, Extended Release	2	FESOTERODINE FUMARATE, Toviaz
TABLET, Extended Release	1	Fesoterodine Fumarate

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