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tolterodine SR, overactive bladder

Pfizer's Upjohn has merged with Mylan to form Viatris Inc. · FDA-approved active Small molecule ✓ Verified May 2026 Quality 5/100

tolterodine SR, overactive bladder is a Small molecule drug developed by Pfizer's Upjohn has merged with Mylan to form Viatris Inc.. It is currently FDA-approved.

Tolterodine SR is a small molecule medication used to treat overactive bladder, as well as other urinary incontinence conditions such as mixed urinary incontinence and stress urinary incontinence. It is available under various brand names, including DETROL and DETROL LA.

At a glance

Generic nametolterodine SR, overactive bladder
SponsorPfizer's Upjohn has merged with Mylan to form Viatris Inc.
ModalitySmall molecule
PhaseFDA-approved

Approved indications

No approved indications tracked.

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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Frequently asked questions about tolterodine SR, overactive bladder

What is tolterodine SR, overactive bladder?

tolterodine SR, overactive bladder is a Small molecule drug developed by Pfizer's Upjohn has merged with Mylan to form Viatris Inc..

Who makes tolterodine SR, overactive bladder?

tolterodine SR, overactive bladder is developed and marketed by Pfizer's Upjohn has merged with Mylan to form Viatris Inc. (see full Pfizer's Upjohn has merged with Mylan to form Viatris Inc. pipeline at /company/pfizer-s-upjohn-has-merged-with-mylan-to-form-viatris-inc).

What development phase is tolterodine SR, overactive bladder in?

tolterodine SR, overactive bladder is FDA-approved (marketed).

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing