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Renacidin (GLUCONOLACTONE)

United Guardian · FDA-approved approved Small molecule Quality 33/100

Renacidin (generic name: GLUCONOLACTONE) is a Calculi Dissolution Agent [EPC] Small molecule drug developed by United Guardian. It is currently FDA-approved (first approved 1990) for Urinary bladder stone.

At a glance

Generic nameGLUCONOLACTONE
SponsorUnited Guardian
Drug classCalculi Dissolution Agent [EPC]
TargetGlucosylceramidase
ModalitySmall molecule
Therapeutic areaUrology
PhaseFDA-approved
First approval1990

Approved indications

Common side effects

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
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results

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Frequently asked questions about Renacidin

What is Renacidin?

Renacidin (GLUCONOLACTONE) is a Calculi Dissolution Agent [EPC] drug developed by United Guardian, indicated for Urinary bladder stone.

What is Renacidin used for?

Renacidin is indicated for Urinary bladder stone.

Who makes Renacidin?

Renacidin is developed and marketed by United Guardian (see full United Guardian pipeline at /company/united-guardian).

What is the generic name of Renacidin?

GLUCONOLACTONE is the generic (nonproprietary) name of Renacidin.

What drug class is Renacidin in?

Renacidin belongs to the Calculi Dissolution Agent [EPC] class. See all Calculi Dissolution Agent [EPC] drugs at /class/calculi-dissolution-agent-epc.

When was Renacidin approved?

Renacidin was first approved on 1990.

What development phase is Renacidin in?

Renacidin is FDA-approved (marketed).

What are the side effects of Renacidin?

Common side effects of Renacidin include Bladder irritability, Chemical cystitis, Transient burning sensation in the bladder.

What does Renacidin target?

Renacidin targets Glucosylceramidase and is a Calculi Dissolution Agent [EPC].

Related

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