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Colestipol

Colestipol is a nonabsorbable anion exchange resin and bile acid sequestrant medication approved by the U.S. Food and Drug Administration (FDA) in 1977 for the treatment of primary hypercholesterolemia in patients who do not respond adequately to dietary measures alone.^[1] It works by binding bile acids in the intestine, forming insoluble complexes that are excreted in the feces, which depletes the body's bile acid pool and prompts the liver to increase expression of low-density lipoprotein (LDL) receptors, thereby lowering serum LDL cholesterol levels by 12% to 24% with typical daily doses of 4 to 16 grams.^[1] This mechanism helps reduce the risk of coronary artery disease and other cardiovascular events associated with elevated cholesterol.^[1]^[2] As an adjunctive therapy, colestipol is often used in combination with statins, niacin, or ezetimibe to achieve greater LDL reductions, such as up to 52% when paired with simvastatin, and it is prescribed alongside lifestyle modifications like a low-fat diet and exercise.^[1] It is available in oral formulations, including tablets and granules for suspension, with dosing typically ranging from 2 to 30 grams per day divided into multiple administrations, often mixed with liquids or foods to improve palatability.^[2]^[3] Due to its negligible systemic absorption (less than 0.17% excreted in urine), colestipol primarily exerts local effects in the gastrointestinal tract and is excreted almost entirely in the feces.^[1] While primarily indicated for hyperlipidemia, colestipol has off-label applications, including relief of cholestatic pruritus in chronic liver disease, management of digoxin toxicity, and potential use as a phosphate binder in hemodialysis patients.^[1] Common adverse effects are gastrointestinal, such as constipation, bloating, nausea, and flatulence, which contribute to its relatively poor long-term tolerability compared to newer lipid-lowering agents.^[1]^[3] Precautions include avoiding concurrent administration with other medications (which should be taken at least one hour before or four hours after colestipol to prevent binding interactions) and monitoring for rare severe effects like gastrointestinal obstruction or bleeding.^[2]^[3]

Medical uses

Indications

Colestipol is primarily approved by the FDA as an adjunct to dietary therapy for the reduction of elevated serum total cholesterol and low-density lipoprotein cholesterol (LDL-C) levels in patients with primary hypercholesterolemia who do not achieve adequate control through diet alone.^[4] This indication targets individuals with elevated LDL-C as the predominant lipid abnormality, where colestipol helps lower LDL-C by approximately 15-30% in clinical settings, based on evidence from trials evaluating bile acid sequestrants.^[5] It is generally not associated with significant reductions in triglycerides and may even elevate them in some patients with baseline hypertriglyceridemia.^[4] In line with 2018 ACC/AHA cholesterol management guidelines (updated 2022), bile acid sequestrants like colestipol are recommended as adjunctive therapy for further LDL-C reduction in high-risk patients on maximally tolerated statins, particularly when triglycerides are below 200 mg/dL, in statin-intolerant individuals, or during pregnancy.^[6]^[7] As part of a broader strategy for managing atherosclerotic cardiovascular disease (ASCVD), colestipol is used within comprehensive risk factor interventions for patients at high risk due to hypercholesterolemia, including those with established coronary heart disease (CHD) or multiple risk factors such as diabetes, hypertension, smoking, or family history of premature CHD. Treatment initiation should include concurrent lifestyle modifications (diet and exercise) with pharmacologic therapy per 2018 ACC/AHA guidelines, particularly for high-risk patients, though the FDA indication specifies adjunct to diet after inadequate response.^[4]^[6] Off-label applications include its use in familial hypercholesterolemia (FH), a genetic form of primary hypercholesterolemia, where clinical studies have demonstrated efficacy in reducing LDL-C levels in children, adolescents, and adults, often in combination regimens.^[8] Additionally, colestipol is sometimes combined with statins (HMG-CoA reductase inhibitors) to achieve enhanced LDL-C reductions beyond monotherapy, with trials showing up to 52% decreases when paired with simvastatin, though such uses are guided by individual patient needs rather than formal approval.^[1] Patient selection for colestipol emphasizes adults with clinical ASCVD or high-risk primary prevention (e.g., diabetes, LDL-C ≥190 mg/dL with no other risk factors) who require further LDL-C reduction despite maximally tolerated statin therapy, per 2018 ACC/AHA guidelines. It is not typically a first-line agent due to potential gastrointestinal tolerability issues, reserving it for cases where statins are insufficient or contraindicated.^[1]^[6]

Dosage and administration

Colestipol is available in two oral forms: tablets containing 1 gram of micronized colestipol hydrochloride each and granules containing 5 grams per packet or level scoopful (unflavored or flavored varieties).^[4] The initial adult dose is 5 grams per day for granules (administered as one dose once or twice daily) or 2 grams per day for tablets (one or two tablets once or twice daily), typically divided with meals to improve tolerability.^[4] Doses should be titrated upward in increments of 5 grams for granules or 2 grams for tablets at intervals of one to two months based on lipid response, with a maximum daily dose of 30 grams for granules (up to six packets or scoopfuls) or 16 grams for tablets (up to 16 tablets).^[4] Administration should occur with food and at least 90 mL (3 ounces) of liquid, such as water, juice, or milk, to minimize gastrointestinal irritation; tablets must be swallowed whole without crushing or chewing, while granules can be mixed into beverages, applesauce, cereal, soup, or pulpy fruits but should not be taken dry or hot.^[4] Other medications should be taken at least one hour before or four hours after colestipol to prevent binding and reduced absorption.^[4] Monitoring involves assessing serum lipid levels, including LDL cholesterol, every four to twelve weeks initially and then periodically every three to six months as per 2018 ACC/AHA guidelines, with dose adjustments based on response and gastrointestinal tolerance.^[4]^[6] In special populations, doses should be reduced in elderly patients or those with a history of constipation—starting granules at 5 grams once daily for five to seven days before increasing—to mitigate risks of gastrointestinal effects; colestipol is not recommended for children under 10 years due to lack of established safety and efficacy.^[4]^[9]

Pharmacology

Mechanism of action

Colestipol is a bile acid sequestrant classified as a high-molecular-weight, nonabsorbable anion-exchange copolymer composed of diethylenetriamine and 1-chloro-2,3-epoxypropane.^[1]^[10] Its primary mechanism involves binding negatively charged bile acids in the intestinal lumen, forming an insoluble, nonabsorbable complex that is excreted in the feces.^[11]^[12] This binding interrupts the normal enterohepatic recirculation of bile acids, where approximately 95% are typically reabsorbed and returned to the liver via the portal vein, thereby increasing fecal bile acid loss.^[1] The depletion of the hepatic bile acid pool triggers compensatory mechanisms in the liver. Specifically, it upregulates the enzyme cholesterol 7α-hydroxylase (CYP7A1), the rate-limiting step in bile acid synthesis, promoting de novo production of bile acids from cholesterol stored in the liver.^[11]^[13] This process also enhances the expression of hepatic low-density lipoprotein (LDL) receptors, which increases the uptake of LDL cholesterol (LDL-C) from the bloodstream to replenish the hepatic cholesterol pool for ongoing bile acid synthesis.^[1]^[12] As a result, circulating LDL-C levels are reduced, while total serum cholesterol decreases due to the net shift in cholesterol metabolism toward bile acid production and excretion.^[14]^[15] Clinical studies demonstrate that colestipol monotherapy typically reduces LDL-C by 12-24% and total cholesterol by about 14% at doses of 4-16 g/day, with minimal effects on high-density lipoprotein cholesterol (HDL-C).^[1]^[14] Triglyceride levels may increase by up to 10% or remain unchanged, particularly in patients with baseline hypertriglyceridemia.^[16]^[17] Colestipol acts exclusively within the gastrointestinal tract, with no systemic absorption, ensuring its effects are localized to the intestinal lumen without entering the bloodstream.^[11]

Pharmacokinetics

Colestipol exhibits negligible systemic absorption, with less than 0.17% of a radiolabeled dose excreted in the urine following 60 days of daily administration at 20 g, due to its high molecular weight and insolubility in water (99.75%).^[4] As an insoluble polymer, it remains primarily within the gastrointestinal tract, where it exerts its effects without entering the bloodstream.^[1] Distribution of colestipol is confined to the intestinal lumen, with no significant plasma concentrations or systemic spread, as it binds bile acids locally in the gut.^[4] This localized action prevents any notable tissue distribution beyond the site of administration.^[1] Colestipol undergoes no metabolism in the body, remaining chemically inert and not hydrolyzed by digestive enzymes.^[4] It forms stable, insoluble complexes with bile acids rather than being biotransformed.^[1] Excretion occurs almost entirely via the feces as the bile acid-colestipol complex, thereby interrupting the enterohepatic recirculation of bile acids.^[4] Trace amounts of unbound components may appear in urine, but this represents minimal systemic exposure.^[1] Due to its lack of absorption, colestipol has no applicable plasma half-life; however, the onset of LDL cholesterol reduction typically begins within 24 to 48 hours of therapy, with maximal effects achieved after approximately 1 month.^[18] The pharmacokinetics of colestipol are influenced by gastrointestinal transit time, which affects the efficiency of bile acid binding in the intestinal lumen, while no issues with dose proportionality arise given its non-absorbable nature.^[1]

Safety profile

Adverse effects

Colestipol, a bile acid sequestrant, is associated with a range of adverse effects, predominantly affecting the gastrointestinal tract, due to its mechanism of binding bile acids in the intestine. These effects are generally mild and dose-related, with constipation being the most frequent complaint.^[4] Bloating, flatulence, abdominal pain, and nausea are also common, and often resolve with dose adjustment or supportive measures.^[1] Less common adverse effects include paradoxical diarrhea, heartburn, anorexia, and exacerbation of hemorrhoids, which may involve minor bleeding.^[4]^[1] Rare effects encompass skin rash, urticaria, and transient elevations in liver enzymes such as AST and ALT.^[4] With long-term use, colestipol can interfere with the absorption of fat-soluble vitamins (A, D, E, and K), potentially leading to deficiencies that manifest as bleeding tendencies from hypoprothrombinemia or, indirectly, increased osteoporosis risk due to vitamin D depletion. Prolonged use may also lead to hyperchloremic metabolic acidosis.^[4]^[1] Supplementation of these vitamins is recommended for patients on prolonged therapy to mitigate such risks.^[1] Serious adverse effects are uncommon but include fecal impaction or bowel obstruction in cases of severe constipation, particularly in elderly or debilitated patients, and worsening of hypertriglyceridemia in those with pre-existing elevations.^[4]^[1] Management strategies focus on prevention and symptom relief: initiating therapy at low doses (e.g., 2 g/day) and titrating gradually minimizes gastrointestinal disturbances; increasing dietary fiber and fluid intake, along with stool softeners, effectively controls constipation in most cases.^[4] Lipid profiles should be monitored periodically, especially in patients prone to triglyceride increases, and dose reduction or discontinuation may be necessary if severe effects persist.^[1]

Contraindications

Colestipol is contraindicated in patients with known hypersensitivity to the drug or any of its components, as this can lead to severe allergic reactions.^[4] Use is not recommended in cases of complete biliary obstruction, as there are no bile acids available for the drug to bind, rendering it ineffective.^[1] Relative contraindications include hypertriglyceridemia with serum triglyceride levels exceeding 400 mg/dL, as colestipol may further elevate triglycerides in such patients and is not recommended for use.^[4] Additionally, formulations containing aspartame, such as certain flavored granules, should be avoided in individuals with phenylketonuria (PKU) due to the phenylalanine content, which can worsen the condition.^[19] Colestipol has minimal systemic absorption and is not expected to cause direct fetal harm based on animal studies; however, it may interfere with maternal absorption of fat-soluble vitamins, potentially posing indirect risks to fetal development. Use during pregnancy only if the potential benefits outweigh these hazards.^[4]^[9] During breastfeeding, caution is advised because colestipol may reduce the mother's absorption of fat-soluble vitamins, potentially affecting the nutritional quality of breast milk and indirectly impacting the infant.^[4] Colestipol is not approved for use in children, and safety and efficacy data are limited in the pediatric population, necessitating avoidance unless under specialist supervision.^[4] It should also be avoided in patients with acute gastrointestinal conditions, such as dysphagia, or a history of severe constipation, as the drug can exacerbate these issues, leading to risks like esophageal obstruction or fecal impaction.^[4]^[1]

Interactions

Drug interactions

Colestipol, as a non-absorbed anion exchange resin, primarily interacts with other medications by binding to them in the gastrointestinal tract, which can reduce their bioavailability and efficacy.^[12] This binding occurs due to colestipol's affinity for anions, leading to recommendations to separate administration of colestipol from other oral drugs by at least 1 hour before or 4 hours after to minimize interference.^[9] Because colestipol is not systemically absorbed, it does not participate in cytochrome P450 (CYP) enzyme interactions.^[1] Significant interactions have been reported with fat-soluble vitamins (A, D, E, and K), where colestipol can impair their absorption, potentially leading to deficiencies with long-term use; supplementation is advised, with vitamins taken at least 1 hour before or 4 hours after colestipol.^[11] Thyroid hormones such as levothyroxine may have decreased absorption, necessitating dose adjustments and monitoring of thyroid-stimulating hormone (TSH) levels.^[9] Cardiac glycosides like digoxin can experience reduced bioavailability, requiring therapeutic drug level monitoring, though results are conflicting.^[12] With HMG-CoA reductase inhibitors (statins), such as lovastatin or simvastatin, colestipol may decrease their absorption if administered concurrently; statins should be taken at least 4 hours before colestipol to avoid this effect, though the combination is often used for enhanced lipid-lowering when timed appropriately.^[11] Anticoagulants like warfarin may have variable interactions: colestipol can bind warfarin directly, reducing its absorption, but it may also impair dietary vitamin K absorption, potentially potentiating warfarin's anticoagulant effect; international normalized ratio (INR) monitoring is essential.^[20] Beta-blockers (e.g., propranolol) and antibiotics such as tetracycline show decreased absorption with colestipol, with propranolol's time to maximum concentration delayed by about 30 minutes and tetracycline requiring at least 1 hour before or 4 hours after colestipol.^[12] In cases of potential interactions, clinical impact often involves dose adjustments, alternative administration schedules, or enhanced monitoring of drug levels and clinical response to ensure efficacy of the co-administered medication.^[1]

Dietary considerations

Colestipol is used as an adjunct to dietary therapy for managing hypercholesterolemia, where a low-cholesterol, low-fat diet is essential for optimal efficacy. Per current guidelines such as the 2025 ACC/AHA and AACE recommendations, treatment integrates intensive lifestyle modifications including reduced intake of saturated fats and cholesterol to lower low-density lipoprotein (LDL) levels synergistically with the drug, without a mandatory pre-treatment delay.^[21]^[22] Incorporating soluble fibers, such as those from oats or psyllium, and plant sterols or stanols from fortified foods can further enhance cholesterol reduction by inhibiting intestinal absorption, complementing colestipol's bile acid-binding mechanism. Patients should follow personalized dietary plans prescribed by healthcare providers, potentially including weight management if overweight, as excess body weight can diminish the drug's effectiveness.^[3] For administration, colestipol tablets are typically taken before meals in divided doses to improve tolerability, while granules should be mixed with at least 3 ounces (90 mL) of water, juice, milk, or other non-carbonated liquids to ensure proper dispersion and prevent esophageal irritation.^[2] Granules can also be blended into pulpy fruits, thin soups, or breakfast cereals for better palatability, though they must not be taken dry to avoid choking or inhalation risks.^[19] This food-compatible mixing aids binding of bile acids in the gastrointestinal tract and reduces gastrointestinal discomfort, but patients should avoid excessive foaming mixtures like those with carbonated beverages.^[23] To mitigate constipation, a common side effect, patients are advised to maintain increased fluid intake—typically at least 1.5 to 2 liters per day—alongside a high-fiber diet rich in fruits, vegetables, and whole grains.^[16] These measures, recommended as the initial approach for managing bowel issues, promote regular stool passage and enhance overall gastrointestinal tolerance during therapy.^[4] Long-term use of colestipol may impair absorption of fat-soluble vitamins (A, D, E, and K) due to bile acid sequestration, necessitating routine supplementation in at-risk patients, such as those with malabsorption or nutritional deficiencies.^[1] Vitamins should be administered at least one hour before or four hours after colestipol doses to minimize interference, with periodic monitoring of serum levels advised.^[9] Colestipol has no direct pharmacokinetic interactions with alcohol or caffeine, but excessive alcohol consumption may exacerbate gastrointestinal irritation or constipation, warranting moderation and symptom monitoring.^[24] Patients should consult healthcare providers regarding any special diets or habits to ensure compatibility with therapy.^[25]

Chemistry

Chemical structure

Colestipol is a water-insoluble, high-molecular-weight anion-exchange resin formed as a copolymer of diethylenetriamine (DETA) and epichlorohydrin (ECH).^[26] This polymeric structure arises from the cross-linked nature of the copolymer, where approximately one in five amine groups from DETA becomes quaternized during synthesis, providing positively charged sites balanced by chloride counterions.^[27] The polymer lacks a fixed molecular weight due to its variable chain length and cross-linking density, a high molecular weight polymer exceeding 1,000,000 daltons, rendering it non-absorbable in the gastrointestinal tract.^[4]^[26] The synthesis of colestipol involves condensation polymerization of DETA and ECH in an aqueous medium, a step-growth process that links the amine functionalities of DETA with the epoxide and chloromethyl groups of ECH to form the extended resin network.^[28] This reaction generates the quaternary ammonium sites inherent to the structure, which contribute to its ion-exchange properties.^[26] The resulting product is then converted to the hydrochloride salt form, colestipol HCl, to enhance stability and solubility in formulation processes without altering its insolubility in water or organic solvents.^[29] In pharmaceutical preparations, colestipol HCl is available as micronized powder for compression into tablets, improving dispersibility and uniformity.^[4] Granular forms are often flavored, such as with orange essence, to enhance palatability when suspended in liquids for oral administration.^[30] Pharmaceutical-grade colestipol meets purity standards exceeding 95% active content, ensuring consistency and efficacy while maintaining its characteristic insolubility in aqueous and organic media.^[31]

Physical properties

Colestipol hydrochloride is available in formulations as a light yellow, water-insoluble resin, with granules appearing as yellow to orange beads and tablets as light yellow, oval, film-coated, tasteless, and odorless solids.^[4]^[30] The compound is hydrophilic yet virtually insoluble in water (99.75%) and common organic solvents, but it swells significantly in aqueous fluids to form a gel-like suspension.^[4]^[30] It is hygroscopic and requires storage in tight containers to protect from moisture.^[4]^[30] Colestipol hydrochloride exhibits stability at controlled room temperature (15–25°C or 20–25°C), decomposing above 260°C without melting, and should be kept away from heat, direct sunlight, and humidity to maintain integrity.^[4]^[30] A 10% (w/w) suspension in water has a pH of 6.0 to 7.5, reflecting its neutral to slightly basic nature due to protonated amine groups.^[30]^[32] In tablet formulations, colestipol is micronized to enhance dispersibility, while granules consist of particles approximately 0.05–0.5 mm in size for facile mixing in liquids.^[4]^[33]

Development and availability

History

Colestipol was developed in the late 1960s by the Upjohn Company as a bile acid sequestrant intended to lower cholesterol levels, building on earlier research into similar agents like cholestyramine. The compound, a high-molecular-weight copolymer of diethylenetriamine and epichlorohydrin, was patented under US Patent 3,692,895, issued on September 19, 1972, which covered its use in treating hypercholesterolemia and pharmaceutically elegant dosage forms. This innovation aimed to address the limitations of existing therapies by providing an insoluble resin that binds bile acids in the intestine, promoting their excretion and thereby reducing circulating low-density lipoprotein (LDL) cholesterol. Early preclinical and clinical evaluations focused on its lipid-lowering potential, positioning it as a non-systemic alternative for managing hyperlipidemia. Pivotal clinical trials in the 1970s demonstrated colestipol's efficacy in reducing serum cholesterol. A randomized study involving 66 hypercholesterolemic patients showed that 10 g of colestipol hydrochloride twice daily lowered total serum cholesterol by an average of 19% over baseline, with comparable reductions in LDL cholesterol. The U.S. Food and Drug Administration (FDA) approved colestipol hydrochloride granules for oral suspension (NDA 017563) on June 1, 1977, marking its entry as an adjunctive therapy for primary hypercholesterolemia. Tablets (NDA 020222) followed in 1994, offering improved patient compliance over the granular form. These approvals were supported by data from controlled trials confirming significant LDL reductions without systemic absorption. Long-term safety and cardiovascular benefits for bile acid sequestrants, including colestipol, were bolstered by the Lipid Research Clinics Coronary Primary Prevention Trial (LRC-CPPT), published in 1984, which used cholestyramine but established class-wide evidence of risk reduction. The trial reported a 19% lower incidence of coronary heart disease events with cholesterol-lowering therapy, linking bile acid binding to decreased cardiovascular disease (CVD) morbidity in high-risk men. Colestipol's original patent expired in 1989, paving the way for generic development, though market entry was delayed until the mid-2000s. The introduction of statins in the late 1980s and their widespread adoption in the 1990s led to a decline in colestipol's clinical use, as these agents offered greater LDL reductions and better tolerability. Despite this shift, colestipol retained relevance for statin-intolerant patients or as combination therapy. The first generic approval came in 2006, when Impax Laboratories received FDA clearance for colestipol hydrochloride tablets (ANDA 077510), granting 180-day exclusivity and increasing accessibility.

Regulatory status and brands

Colestipol hydrochloride is approved by the United States Food and Drug Administration (FDA) as a prescription medication for use as adjunctive therapy to diet for the reduction of elevated low-density lipoprotein cholesterol in patients with primary hypercholesterolemia who do not respond adequately to diet or other lipid-lowering measures.^[1] The original new drug applications were approved by The Upjohn Company (now part of Pfizer): NDA 017563 for granules on April 4, 1977, and NDA 020222 for Colestid tablets on July 19, 1994.^[34]^[35] Generic versions of colestipol hydrochloride tablets became available following FDA approval of the first abbreviated new drug application (ANDA) in October 2006 by Impax Laboratories (now Amneal Pharmaceuticals), which included 180-day market exclusivity.^[36] Additional ANDA approvals have followed, including one in April 2023 by ANI Pharmaceuticals for 1 g tablets.^[37] Internationally, colestipol is approved in Canada as Colestid tablets and granules for oral suspension, regulated by Health Canada as a prescription drug for hypercholesterolemia management.^[38] In Australia, colestipol hydrochloride (as Colestid granules) was previously registered with the Therapeutic Goods Administration but had its registration cancelled under section 30(1)(c) of the Therapeutic Goods Act in October 2020.^[39] In the European Union, colestipol is not centrally authorized by the European Medicines Agency but is available through national marketing authorizations in select member states, such as Lestid in Spain and Cholestabyl in other regions.^[11] Colestipol is not included on the World Health Organization's Model List of Essential Medicines.^[40] The primary brand name for colestipol is Colestid, originally developed and marketed by Pfizer (formerly Upjohn), available in the United States as micronized hydrochloride tablets (1 g) and flavored granules for oral suspension.^[4] Generic formulations of colestipol hydrochloride are widely available in tablet and granule forms, with no over-the-counter options approved in major markets; it remains a prescription-only medication globally.^[41] In lipid management guidelines, such as the 2022 American College of Cardiology Expert Consensus Decision Pathway on non-statin therapies, bile acid sequestrants including colestipol are recommended (Class 2a) for high-risk patients with atherosclerotic cardiovascular disease who are statin-intolerant or require additional LDL-C lowering beyond maximally tolerated statins.^[7] As a low-cost generic, colestipol is accessible and affordable, with average U.S. retail prices for generic 1 g tablets ranging from $0.42 to $0.50 per tablet (or per gram equivalent), often lower with discount programs.^[42] It is available exclusively in oral formulations, with no injectable or other delivery methods approved.^[43]

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The WHO Model Lists of Essential Medicines are updated every two years by the Expert Committee on Selection and Use of Essential Medicines.Missing: Colestipol | Show results with:Colestipol
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https://investors.amneal.com/news/press-releases/press-release-details/2006/IMPAX-Receives-FDA-Approval-for-Generic-Version-of-ColestidR-Tablets/default.aspx
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2022 ACC Expert Consensus Decision Pathway on the Role ... - JACC
The 2018 AHA/ACC/multisociety cholesterol guideline indicates that calcium scoring may be considered in select patients at borderline or intermediate risk (≥5.0 ...
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https://dhpp.hpfb-dgpsa.ca/dhpp/resource/18627
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Generic Colestid Availability - Drugs.com
Oct 8, 2025 · Yes, the FDA has approved a generic version of Colestid. However, FDA approval doesn't guarantee the generic will be available in pharmacies.Missing: NDA | Show results with:NDA