Colchicinedrug info

colchicine 0.5 MG / probenecid 500 MG Oral Tablet

What it is used for

INDICATIONS & USAGE For the treatment of chronic gouty arthritis when complicated by frequent, recurrent acute attacks of gout.

Text above is quoted in full from the FDA-approved drug label published by openFDA, effective January 27, 2026. Matched to this product by RxNorm code. Cross-references to other sections of the full prescribing information have been removed, since they point to a document not shown here. Nothing else is changed: no sentence is shortened, reworded or summarised.

Description

Probenecid and colchicine contains probenecid, which is a uricosuric agent, and colchicine, which has antigout activity, the mechanism of which is unknown. Probenecid is the generic name for p-(Dipropylsulfamoyl)benzoic acid. The structural formula is represented below: C 13 H 19 NO 4 S M.W.285.36 Probenecid is a white or practically white, fine, crystalline powder. It is soluble in dilute alkali, in alcohol, in chloroform, and in acetone; it is practically insoluble in water and in dilute acids. Colchicine is an alkaloid obtained from various species of Colchicum. The chemical name for Colchicine is (S)-N-(5,6,7,9- tetrahydro-1,2,3,10-tetramethoxy-9-oxobenzo[α]heptalen-7-yl) acetamide. The structural formula is represented below: C 22 H 25 NO 6 M.W.399.44 Colchicine consists of yellowish white to pale yellow to pale greenish-yellow powder which darken on exposure to light. Colchicine is freely soluble in chloroform. Each tablet for oral administration contains 500 mg of probenecid and 0.5 mg of colchicine. Each tablet also contains the following inactive ingredients: colloidal silicon dioxide, corn starch, magnesium stearate, microcrystalline cellulose, povidone, sodium lauryl sulfate and sodium starch glycolate. FDA approved dissolution test specifications differ from the USP. probenecid-struc.jpg colchicine-struc.jpg

Text above is quoted in full from the FDA-approved drug label published by openFDA, effective January 27, 2026. Matched to this product by RxNorm code. Cross-references to other sections of the full prescribing information have been removed, since they point to a document not shown here. Nothing else is changed: no sentence is shortened, reworded or summarised.

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