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Renacidin (CITRIC ACID)

Baxter · FDA-approved approved Small molecule Quality 50/100

Renacidin (generic name: CITRIC ACID) is a Anti-coagulant Small molecule drug developed by Baxter. It is currently FDA-approved (first approved 1982) for Calcium Phosphate Renal Calculi, Headache disorder, Indigestion.

Renacidin works by inhibiting the formation of calcium oxalate crystals in the urine, which can help prevent kidney stones.

At a glance

Generic nameCITRIC ACID
SponsorBaxter
Drug classAnti-coagulant
ModalitySmall molecule
Therapeutic areaNeuroscience
PhaseFDA-approved
First approval1982

Mechanism of action

XENLETA is an antibacterial drug [see Microbiology (12.4)].

Approved indications

Common side effects

Key clinical trials

Patents

PatentExpiryType

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
FDA Orange BookPatents + exclusivity

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Frequently asked questions about Renacidin

What is Renacidin?

Renacidin (CITRIC ACID) is a Anti-coagulant drug developed by Baxter, indicated for Calcium Phosphate Renal Calculi, Headache disorder, Indigestion.

How does Renacidin work?

Renacidin works by inhibiting the formation of calcium oxalate crystals in the urine, which can help prevent kidney stones.

What is Renacidin used for?

Renacidin is indicated for Calcium Phosphate Renal Calculi, Headache disorder, Indigestion, Pain, Struvite Renal Calculi.

Who makes Renacidin?

Renacidin is developed and marketed by Baxter (see full Baxter pipeline at /company/baxter).

What is the generic name of Renacidin?

CITRIC ACID is the generic (nonproprietary) name of Renacidin.

What drug class is Renacidin in?

Renacidin belongs to the Anti-coagulant class. See all Anti-coagulant drugs at /class/anti-coagulant.

When was Renacidin approved?

Renacidin was first approved on 1982.

What development phase is Renacidin in?

Renacidin is FDA-approved (marketed).

What are the side effects of Renacidin?

Common side effects of Renacidin include Administration site reactions, Diarrhea, Hepatic enzyme elevation, Nausea, Hypokalemia, Insomnia.

Related

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