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Molecule

Oxaprozin

Anti-Inflammatory Agents
Available on requestRheumatology
Presentations
3
Brands
1
Manufacturers
1
Available from stock
0

Oxaprozin is a nonsteroidal anti-inflammatory drug. It is available as tablets and capsules for oral use. MedsAcross supplies Oxaprozin for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Key facts

Pharmacological class
Anti-Inflammatory Agents, Nonsteroidal Anti-inflammatory Drug, Cyclooxygenase Inhibitors
ATC classification
M01AE12 Oxaprozin · Anti-inflammatory and antirheumatic medicines, subgroup M01A, subgroup M01AE
US FDA first approval
29 October 1992
EU status
Not recorded
Orphan designation
Not recorded
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Oral
Dosage forms
Tablet, Capsule
Identifiers
UNII MHJ80W9LRBRxCUI 32613CAS 21256-18-8DrugBank DB00991Q1749609

Clinical information

From the regulator-approved product information. Each section names its source.

Uses

OXAPROZIN is indicated: For relief of the signs and symptoms of osteoarthritis For relief of the signs and symptoms of rheumatoid arthritis For relief of the signs and symptoms of juvenile rheumatoid arthritis OXAPROZIN CAPSULES is a non-steroidal anti-inflammatory drug indicated for: Relief of signs and symptoms of Osteoarthritis (OA). Relief of signs and symptoms of Rheumatoid Arthritis (RA). Relief of signs and symptoms of Juvenile Rheumatoid Arthritis (JRA)

Source: US FDA prescribing information

How it works

Oxaprozin has analgesic, anti-inflammatory, and antipyretic properties. The mechanism of action of OXAPROZIN CAPSULES, like that of other NSAIDs, is not completely understood but involves inhibition of cyclooxygenase (COX-1 and COX-2). Oxaprozin is a potent inhibitor of prostaglandin synthesis in vitro. Oxaprozin concentrations reached during therapy have produced in vivo effects. Prostaglandins sensitize afferent nerves and potentiate the action of bradykinin in inducing pain in animal models. Prostaglandins are mediators of inflammation. Because oxaprozin is an inhibitor of prostaglandin synthesis, its mode of action may be due to a decrease of prostaglandins in peripheral tissues.

Source: US FDA prescribing information

Dosing overview

Use the lowest effective dosage for shortest duration consistent with individual patient treatment goals. OA: 1200 mg (four 300 mg caplets) given orally once a day. RA: 1200 mg (four 300 mg caplets) given orally once a day. JRA: 600 mg (two 300 mg capsules) once daily in patients 22 to 31 kg. 900 mg (three 300 mg capsules) once daily in patients 32 to 54 kg. 1,200 mg (four 300 mg capsules) once daily in patients 55 kg or greater.

Source: US FDA prescribing information

Contraindications

OXAPROZIN CAPSULES is contraindicated in the following patients: Known hypersensitivity (e.g., anaphylactic reactions and serious skin reactions) to oxaprozin or any components of the drug product History of asthma, urticaria, or other allergic-type reactions after taking aspirin or other NSAIDs. Severe, sometimes fatal, anaphylactic reactions to NSAIDs have been reported in such patients In the setting of CABG surgery Known hypersensitivity to oxaprozin or any components of the drug product. History of asthma, urticaria, or other allergic-type reactions after taking aspirin or other NSAIDs. In the setting of CABG surgery

Source: US FDA prescribing information

Warnings and precautions

Warning: RISK OF SERIOUS CARDIOVASCULAR AND GASTROINTESTINAL EVENTS. WARNING: RISK OF SERIOUS CARDIOVASCULAR AND GASTROINTESTINAL EVENTS Nonsteroidal anti-inflammatory drugs (NSAIDs) cause an increased risk of serious cardiovascular thrombotic events, including myocardial infarction and stroke, which can be fatal. This risk may occur early in treatment and may increase with duration of use. . Hepatotoxicity: Inform patients of warning signs and symptoms of hepatotoxicity. Discontinue if abnormal liver tests persist or worsen or if clinical signs and symptoms of liver disease develop. Hypertension: Patients taking some antihypertensive medications may have impaired response to these therapies when taking NSAIDs. Monitor blood pressure.

Source: US FDA prescribing information

Side effects

The following clinically significant adverse reactions are described elswhere in the labeling: Cardiovascular Thrombotic Events GI Bleeding, Ulceration and Perforation Hepatotoxicity Hypertension Heart Failure and Edema Renal Toxicity and Hyperkalemia Anaphylactic Reactions Serious Skin Reactions Hematologic Toxicity Most common adverse reactions (incidence > 3%) are: constipation, diarrhea, dyspepsia, nausea, rash

Source: US FDA prescribing information

Interactions

See TABLE 2 for clinically significant drug interactions with oxaprozin. Table 2: Clinically Significant Drug Interactions with Oxaprozin Drugs That Interfere with Hemostasis Clinical Impact: Oxaprozin and anticoagulants such as warfarin have a synergistic effect on bleeding. The concomitant use of oxaprozin and anticoagulants have an increased risk of serious bleeding compared to the use of either drug alone. Serotonin release by platelets plays an important role in hemostasis. Case-control and cohort epidemiological studies showed that concomitant use of drugs that interfere with serotonin reuptake and an NSAID may potentiate the risk of bleeding more than an NSAID alone. Intervention: Monitor patients with concomitant use of OXAPROZIN CAPSULES with anticoagulants (e.g., warfarin), antiplatelet drugs (e.g., aspirin), SSRIs, and SNRIs for signs of bleeding.

Source: US FDA prescribing information

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

All presentations

3 presentations of Oxaprozin, sorted by availability.

MedicineManufacturerRegisterAvailability
Oxaprozin 600 mg tabletOralGeneric name—US FDAAvailable on request
Coxanto 300 mg capsuleOralSOLA PharmaceuticalsUS FDAAvailable on request
Oxaprozin 300 mg capsuleOralGeneric name—US FDAAvailable on request

Brands by market

1 brand names across 1 markets.

Brand names by country

United States

Manufacturers

Regulatory status

Approval facts from US FDA, EMA and CDSCO data, and registration status by country where we hold register data.

RegisterStatusSource
US FDAFirst approved 29 October 1992Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Conditions

Conditions linked to Oxaprozin in public data. This is not a list of approved uses, see the clinical information.

Questions and answers

Is Oxaprozin available for export from India?

Yes, on request. MedsAcross lists 3 presentations of Oxaprozin and sources them for licensed hospitals, importers and physicians against valid import documents.

What brand names does Oxaprozin have?

The catalogue lists 1 brand names for Oxaprozin, including Coxanto.

Is Oxaprozin approved by the US FDA?

Yes. The US FDA first approved Oxaprozin on 29 October 1992, according to Drugs@FDA.

Does Oxaprozin need cold chain shipping?

No listed presentation of Oxaprozin is recorded as needing a cold chain. Storage conditions are shown on each presentation page.

Which ATC class is Oxaprozin in?

Oxaprozin is classified under ATC code M01AE12 (Oxaprozin).

References

  1. Oxaprozin prescribing information (SOLA Pharmaceuticals). U.S. National Library of Medicine, DailyMed. Retrieved 3 December 2025

Request Oxaprozin for export supply

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