Oxybutynin — ingredient monograph

Overview

Source: NDC Directory

Ingredient name

OXYBUTYNIN CHLORIDE

Base moiety

OXYBUTYNIN

RxNorm CUI

863619

UNII

L9F3D9RENQ

Medication products

8

Brand names

3

Dosage forms

6

FAERS reports

8,715 · not a risk measure

Products containing this ingredient

Source: NDC Directory 8 products

Oxybutynin Chloride Powder
7 NDC
Oxybutynin Hydrochloride Powder
1 NDC
OXYBUTYNINE HYDROCHLORIDE Oxybutynine Hydrochloride · Powder
1 NDC
oxybutynin Tablet, Film Coated, Extended Release
Rx ANDA TE AB 4 recalls 10 NDC
Oxybutynin Chloride Tablet, Extended Release
Rx ANDA TE AB 2 recalls 51 NDC
Oxybutynin Chloride Tablet
Rx ANDA TE AB 1 recall 50 NDC
Oxybutynin Chloride Syrup
Rx ANDA TE AA 2 NDC
Oxybutynin Chloride Solution
Rx ANDA TE AA 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	3	Oxybutynin Chloride, Oxybutynin Hydrochloride, OXYBUTYNINE HYDROCHLORIDE
TABLET, Film COATED, Extended Release	1	oxybutynin
TABLET, Extended Release	1	Oxybutynin Chloride
Tablet	1	Oxybutynin Chloride
Syrup	1	Oxybutynin Chloride
Solution	1	Oxybutynin Chloride

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