Colchicine


Direct Rx
Human Prescription Drug
NDC 72189-331
Colchicine is a human prescription drug labeled by 'Direct Rx'. National Drug Code (NDC) number for Colchicine is 72189-331. This drug is available in dosage form of Tablet. The names of the active, medicinal ingredients in Colchicine drug includes Colchicine - .6 mg/1 . The currest status of Colchicine drug is Active.

Drug Information:

Drug NDC: 72189-331
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name: Colchicine
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type: Human Prescription Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name: Colchicine
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Direct Rx
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Tablet
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status: Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:COLCHICINE - .6 mg/1
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Marketing Category: ANDA
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Marketing Start Date: 01 Mar, 2022
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 15 Jan, 2026
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Application Number: ANDA209876
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
Listing Expiration Date: 31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Manufacturer Name:Direct Rx
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:197541
The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms.
NUI:N0000182141
N0000000239
N0000193949
M0000713
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:SML2Y3J35T
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class MOA:Cytochrome P450 3A4 Inhibitors [MoA]
P-Glycoprotein Interactions [MoA]
Mechanism of action of the drug—molecular, subcellular, or cellular functional activity—of the drug’s established pharmacologic class. Takes the form of the mechanism of action, followed by `[MoA]` (such as `Calcium Channel Antagonists [MoA]` or `Tumor Necrosis Factor Receptor Blocking Activity [MoA]`.
Pharmacologic Class EPC:Alkaloid [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class CS:Alkaloids [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:Alkaloid [EPC]
Alkaloids [CS]
Cytochrome P450 3A4 Inhibitors [MoA]
P-Glycoprotein Interactions [MoA]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
72189-331-033 TABLET in 1 BOTTLE (72189-331-03)01 Mar, 2022N/ANo
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Product Elements:

Colchicine colchicine hypromellose 2208 (100 mpa.s) polyethylene glycol, unspecified cellulose, microcrystalline titanium dioxide magnesium stearate colchicine colchicine fd&c red no. 40 triacetin fd&c blue no. 2 polydextrose starch, corn sodium starch glycolate type a corn lactose monohydrate y372

Indications and Usage:

1.1 gout flares colchicine tablets are indicated for prophylaxis and the treatment of acute gout flares. • prophylaxis of gout flares: colchicine tablets are indicated for prophylaxis of gout flares. • treatment of gout flares: colchicine tablets are indicated for treatment of acute gout flares when taken at the first sign of a flare. 1.2 familial mediterranean fever (fmf) colchicine tablets are indicated in adults and children four years or older for treatment of familial mediterranean fever (fmf).

Dosage and Administration:

The long-term use of colchicine is established for fmf and the prophylaxis of gout flares, but the safety and efficacy of repeat treatment for gout flares has not been evaluated. the dosing regimens for colchicine tablets are different for each indication and must be individualized. the recommended dosage of colchicine tablets depends on the patient’s age, renal function, hepatic function and use of coadministered drugs [see dosage and administration (2.4, 2.5, 2.6)]. colchicine tablets are administered orally without regard to meals. colchicine tablets are not an analgesic medication and should not be used to treat pain from other causes. 2.1 gout flares prophylaxis of gout flares the recommended dosage of colchicine tablets for prophylaxis of gout flares for adults and adolescents older than 16 years of age is 0.6 mg once or twice daily. the maximum recommended dose for prophylaxis of gout flares is 1.2 mg/day. an increase in gout flares may occur after initiation of uric acid-l
owering therapy, including pegloticase, febuxostat and allopurinol, due to changing serum uric acid levels resulting in mobilization of urate from tissue deposits. colchicine tablets are recommended upon initiation of gout flare prophylaxis with uric acid-lowering therapy. prophylactic therapy may be beneficial for at least the first six months of uric acid-lowering therapy. treatment of gout flares the recommended dose of colchicine tablets for treatment of a gout flare is 1.2 mg (two tablets) at the first sign of the flare followed by 0.6 mg (one tablet) one hour later. higher doses have not been found to be more effective. the maximum recommended dose for treatment of gout flares is 1.8 mg over a 1-hour period. colchicine tablets may be administered for treatment of a gout flare during prophylaxis at doses not to exceed 1.2 mg (two tablets) at the first sign of the flare followed by 0.6 mg (one tablet) one hour later. wait 12 hours and then resume the prophylactic dose. 2.2 fmf the recommended dosage of colchicine tablets for fmf in adults is 1.2 mg to 2.4 mg daily. colchicine tablets should be increased as needed to control disease and as tolerated in increments of 0.3 mg/day to a maximum recommended daily dose. if intolerable side effects develop, the dose should be decreased in increments of 0.3 mg/day. the total daily colchicine tablets dose may be administered in one to two divided doses. 2.3 recommended pediatric dosage prophylaxis and treatment of gout flares colchicine tablets are not recommended for pediatric use in prophylaxis or treatment of gout flares. fmf the recommended dosage of colchicine tablets for fmf in pediatric patients 4 years of age and older is based on age. the following daily doses may be given as a single or divided dose twice daily: • children 4 to 6 years: 0.3 mg to 1.8 mg daily • children 6 to 12 years: 0.9 mg to 1.8 mg daily • adolescents older than 12 years: 1.2 mg to 2.4 mg daily 2.4 dose modification for coadministration of interacting drugs concomitant therapy coadministration of colchicine tablets with drugs known to inhibit cyp3a4 and/or p-glycoprotein (p-gp) increases the risk of colchicine-induced toxic effects (table 1). if patients are taking or have recently completed treatment with drugs listed in table 1 within the prior 14 days, the dose adjustments are as shown in the table below [see drug interactions (7)]. table 1. colchicine tablets dose adjustment for coadministration with interacting drugs if no alternative available* * for magnitude of effect on colchicine plasma concentrations [see clinical pharmacology (12.3)] † patients with renal or hepatic impairment should not be given colchicine tablets in conjunction with strong cyp3a4 or p-gp inhibitors [see contraindications (4)] ‡ when used in combination with ritonavir, see dosing recommendations for strong cyp3a4 inhibitors [see contraindications (4)] strong cyp3a4 inhibitors† gout flares noted or anticipated outcome prophylaxis of gout flares treatment of gout flares fmf drug original intended dosage adjusted dose original intended dosage adjusted dose original intended dosage adjusted dose atazanavir clarithromycin darunavir/ ritonavir‡ indinavir itraconazole ketoconazole lopinavir/ ritonavir nefazodone nelfinavir ritonavir saquinavir telithromycin tipranavir/ ritonavir significant increase in colchicine plasma levels; fatal colchicine toxicity has been reported with clarithromycin, a strong cyp3a4 inhibitor. similarly, significant increase in colchicine plasma levels is anticipated with other strong cyp3a4 inhibitors 0.6 mg twice a day 0.6 mg once a day 0.3 mg once a day 0.3 mg once every other day 1.2 mg (2 tablets) followed by 0.6 mg (1 tablet) 1 hour later. dose to be repeated no earlier than 3 days. 0.6 mg (1 tablet) x 1 dose, followed by 0.3 mg (1/2 tablet) 1 hour later. dose to be repeated no earlier than 3 days. maximum daily dose of 1.2 mg - 2.4 mg maximum daily dose of 0.6 mg (may be given as 0.3 mg twice a day) moderate cyp3a4 inhibitors gout flares note or anticipated outcome prophylaxis of gout flares treatment of gout flares fmf drug original intended dosage adjusted dosage original intended dosage adjusted dosage original intended dosage adjusted dosage amprenavir aprepitant diltiazem erythromycin fluconazole fosamprenavir (prodrug of amprenavir) grapefruit juice verapamil significant increase in colchicine plasma concentration is anticipated. neuromuscular toxicity has been reported with diltiazem and verapamil interactions. 0.6 mg twice a day 0.6 mg once a day 0.3 mg twice a day or 0.6 mg once a day 0.3 mg once a day 1.2 mg (2 tablets) followed by 0.6 mg (1 tablet) 1 hour later. dose to be repeated no earlier than 3 days. 1.2 mg (2 tablets) x 1 dose. dose to be repeated no earlier than 3 days. maximum daily dose of 1.2 mg - 2.4 mg maximum daily dose of 1.2 mg (may be given as 0.6 mg twice a day) p-gp inhibitors gout flares note or anticipated outcome prophylaxis of gout flares treatment of gout flares fmf drug original intended dosage adjusted dosage original intended dosage adjusted dosage original intended dosage adjusted dosage cyclosporine ranolazine significant increase in colchicine plasma levels; fatal colchicine toxicity has been reported with cyclosporine, a p-gp inhibitor. similarly, significant increase in colchicine plasma levels is anticipated with other p-gp inhibitors. 0.6 mg twice a day 0.6 mg once a day 0.3 mg once a day 0.3 mg once every other day 1.2 mg (2 tablets) followed by 0.6 mg (1 tablet) 1 hour later. dose to be repeated no earlier than 3 days. 0.6 mg (1 tablet) x 1 dose. dose to be repeated no earlier than 3 days. maximum daily dose of 1.2 mg - 2.4 mg maximum daily dose of 0.6 mg (may be given as 0.3 mg twice a day) table 2. colchicine tablets dose adjustment for coadministration with protease inhibitors protease inhibitor clinical comment w/ colchicine - prophylaxis of gout flares w/o colchicine – treatment of gout flares w/colchicine – treatment of fmf atazanavir sulfate (reyataz) patients with renal or hepatic impairment should not be given colchicine with reyataz. original dose adjusted dose 0.6 mg (1 tablet) x 1 dose, followed by 0.3 mg (1/2 tablet) 1 hour later. dose to be repeated no earlier than 3 days. maximum daily dose of 0.6 mg (may be given as 0.3 mg twice a day) 0.6 mg twice a day 0.6 mg once a day 0.3 mg once a day 0.3 mg once every other day darunavir (prezista) patients with renal or hepatic impairment should not be given colchicine with prezista/ritonavir. original dose adjusted dose 0.6 mg (1 tablet) x 1 dose, followed by 0.3 mg (1/2 tablet) 1 hour later. dose to be repeated no earlier than 3 days. maximum daily dose of 0.6 mg (may be given as 0.3 mg twice a day) 0.6 mg twice a day 0.6 mg once a day 0.3 mg once a day 0.3 mg once every other day fosamprenavir (lexiva) with ritonavir patients with renal or hepatic impairment should not be given colchicine with lexiva/ritonavir. original dose adjusted dose 0.6 mg (1 tablet) x 1 dose, followed by 0.3 mg (1/2 tablet) 1 hour later. dose to be repeated no earlier than 3 days. maximum daily dose of 0.6 mg (may be given as 0.3 mg twice a day) 0.6 mg twice a day 0.6 mg once a day 0.3 mg once a day 0.3 mg once every other day fosamprenavir (lexiva) patients with renal or hepatic impairment should not be given colchicine with lexiva/ritonavir original dose adjusted dose 1.2 mg (2 tablets) x 1 dose. dose to be repeated no earlier than 3 days. maximum daily dose of 1.2 mg (may be given as 0.6 mg twice a day) 0.6 mg twice a day 0.6 mg once a day 0.3 mg twice a day or 0.6 mg once a day 0.3 mg once a day indinavir (crixivan) patients with renal or hepatic impairment should not be given colchicine with crixivan. original dose adjusted dose 0.6 mg (1 tablet) x 1 dose, followed by 0.3 mg (1/2 tablet) 1 hour later. dose to be repeated no earlier than 3 days. maximum daily dose of 0.6 mg (may be given as 0.3 mg twice a day) 0.6 mg twice a day 0.6 mg once a day 0.3 mg once a day 0.3 mg once every other day lopinavir/ ritonavir (kaletra) patients with renal or hepatic impairment should not be given colchicine with kaletra. original dose adjusted dose 0.6 mg (1 tablet) x 1 dose, followed by 0.3 mg (1/2 tablet) 1 hour later. dose to be repeated no earlier than 3 days. maximum daily dose of 0.6 mg (may be given as 0.3 mg twice a day) 0.6 mg twice a day 0.6 mg once a day 0.3 mg once a day 0.3 mg once every other day nelfinavir mesylate (viracept) patients with renal or hepatic impairment should not be given colchicine with viracept. original dose adjusted dose 0.6 mg (1 tablet) x 1 dose, followed by 0.3 mg (1/2 tablet) 1 hour later. dose to be repeated no earlier than 3 days. maximum daily dose of 0.6 mg (may be given as 0.3 mg twice a day) 0.6 mg twice a day 0.6 mg once a day 0.3 mg once a day 0.3 mg once every other day ritonavir (norvir) patients with renal or hepatic impairment should not be given colchicine with norvir. original dose adjusted dose 0.6 mg (1 tablet) x 1 dose, followed by 0.3 mg (1/2 tablet) 1 hour later. dose to be repeated no earlier than 3 days. maximum daily dose of 0.6 mg (may be given as 0.3 mg twice a day) 0.6 mg twice a day 0.6 mg once a day 0.3 mg once a day 0.3 mg once every other day saquinavir mesylate (invirase) patients with renal or hepatic impairment should not be given colchicine with invirase/ritonavir. original dose adjusted dose 0.6 mg (1 tablet) x 1 dose, followed by 0.3 mg (1/2 tablet) 1 hour later. dose to be repeated no earlier than 3 days. maximum daily dose of 0.6 mg (may be given as 0.3 mg twice a day) 0.6 mg twice a day 0.6 mg once a day 0.3 mg once a day 0.3 mg once every other day tipranavir (aptivus) patients with renal or hepatic impairment should not be given colchicine with aptivus/ritonavir. original dose adjusted dose 0.6 mg (1 tablet) x 1 dose, followed by 0.3 mg (1/2 tablet) 1 hour later. dose to be repeated no earlier than 3 days. maximum daily dose of 0.6 mg (may be given as 0.3 mg twice a day) 0.6 mg twice a day 0.6 mg once a day 0.3 mg once a day 0.3 mg once every other day treatment of gout flares with colchicine tablets is not recommended in patients receiving prophylactic dose of colchicine tablets and cyp3a4 inhibitors. 2.5 dose modification in renal impairment colchicine dosing must be individualized according to the patient's renal function [see use in specific populations (8.6)]. clcr in ml/minute may be estimated from serum creatinine (mg/dl) determination using the following formula: [dosing calculation] gout flares prophylaxis of gout flares for prophylaxis of gout flares in patients with mild (estimated creatinine clearance [clcr] 50 to 80 ml/min) to moderate (clcr 30 to 50 ml/min) renal function impairment, adjustment of the recommended dose is not required, but patients should be monitored closely for adverse effects of colchicine. however, in patients with severe impairment, the starting dose should be 0.3 mg/day and any increase in dose should be done with close monitoring. for the prophylaxis of gout flares in patients undergoing dialysis, the starting doses should be 0.3 mg given twice a week with close monitoring [see clinical pharmacology (12.3), use in specific populations (8.6)]. treatment of gout flares for treatment of gout flares in patients with mild (clcr 50 to 80 ml/min) to moderate (clcr 30 to 50 ml/min) renal function impairment, adjustment of the recommended dose is not required, but patients should be monitored closely for adverse effects of colchicine. however, in patients with severe impairment, while the dose does not need to be adjusted for the treatment of gout flares, a treatment course should be repeated no more than once every two weeks. for patients with gout flares requiring repeated courses, consideration should be given to alternate therapy. for patients undergoing dialysis, the total recommended dose for the treatment of gout flares should be reduced to a single dose of 0.6 mg (one tablet). for these patients, the treatment course should not be repeated more than once every two weeks [see clinical pharmacology (12.3), use in specific populations (8.6)]. treatment of gout flares with colchicine tablets is not recommended in patients with renal impairment who are receiving colchicine tablets for prophylaxis. fmf caution should be taken in dosing patients with moderate and severe renal impairment and in patients undergoing dialysis. for these patients, the dosage should be reduced [see clinical pharmacology (12.3)]. patients with mild (clcr 50 to 80 ml/min) and moderate (clcr 30 to 50 ml/min) renal impairment should be monitored closely for adverse effects of colchicine tablets. dose reduction may be necessary. for patients with severe renal failure (clcr less than 30 ml/min), start with 0.3 mg/day; any increase in dose should be done with adequate monitoring of the patient for adverse effects of colchicine [see use in specific populations (8.6)]. for patients undergoing dialysis, the total recommended starting dose should be 0.3 mg (half tablet) per day. dosing can be increased with close monitoring. any increase in dose should be done with adequate monitoring of the patient for adverse effects of colchicine [see clinical pharmacology (12.3), use in specific populations (8.6)]. 2.6 dose modification in hepatic impairment gout flares prophylaxis of gout flares for prophylaxis of gout flares in patients with mild to moderate hepatic function impairment, adjustment of the recommended dose is not required, but patients should be monitored closely for adverse effects of colchicine. dose reduction should be considered for the prophylaxis of gout flares in patients with severe hepatic impairment [see use in specific populations (8.7)]. treatment of gout flares for treatment of gout flares in patients with mild to moderate hepatic function impairment, adjustment of the recommended dose is not required, but patients should be monitored closely for adverse effects of colchicine. however, for the treatment of gout flares in patients with severe impairment, while the dose does not need to be adjusted, a treatment course should be repeated no more than once every two weeks. for these patients, requiring repeated courses for the treatment of gout flares, consideration should be given to alternate therapy [see use in specific populations (8.7)]. treatment of gout flares with colchicine tablets is not recommended in patients with hepatic impairment who are receiving colchicine tablets for prophylaxis. fmf patients with mild to moderate hepatic impairment should be monitored closely for adverse effects of colchicine. dose reduction should be considered in patients with severe hepatic impairment [see use in specific populations (8.7)]. close

Dosage Forms and Strength:

Colchicine tablets usp, 0.6 mg — purple color, film-coated, capsule shaped tablets debossed with ‘ [logo] 372’ on one side and score line on the other side of the tablet.

Contraindications:

Patients with renal or hepatic impairment should not be given colchicine tablets in conjunction with p-gp or strong cyp3a4 inhibitors (this includes all protease inhibitors except fosamprenavir). in these patients, life-threatening and fatal colchicine toxicity has been reported with colchicine taken in therapeutic doses.

How Supplied:

16.1 how supplied colchicine tablets usp, 0.6 mg are purple colored, film-coated, capsule shaped tablets debossed with ‘stylized y 372’ on one side and score line on the other side of the tablet. bottles of 30 ndc 43598-372-30 bottles of 100 ndc 43598-372-01 bottles of 1,000 ndc 43598-372-10 16.2 storage store at 20° to 25°c (68° to 77°f) [see usp controlled room temperature]. protect from light. dispense in tight, light-resistant container.

Package Label Principal Display Panel:

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