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Two medicines, side by side

Colesevelam vs cholestyramine

Colesevelam and cholestyramine are both labeled for high cholesterol. Drugs@FDA records approvals of colesevelam since 2000 and of cholestyramine since 1973. Pharmacies paid $0.262 per colesevelam 625 mg tablet and $0.834 per packet (Cholestyramine packet) (NADAC, October 7, 2026); the strengths differ, so the two prices are not like for like. How each works, in its label's words: Colesevelam, “Primary Hyperlipidemia: Colesevelam hydrochloride, the active pharmaceutical ingredient, is a non-absorbed, lipid-lowering polymer that binds bile acids in the intestine, impeding their reabsorption.”; Cholestyramine, “and an effect on serum lipids similar to that of cholestyramine for oral suspension) plus either nicotinic acid or lovastatin.”

Check it at the source: the colesevelam FDA label on DailyMed (effective December 28, 2023); the cholestyramine FDA label on DailyMed (effective August 20, 2026).

Highlights of the colesevelam record

Colesevelam (Welchol) · label of December 28, 2023

Used for

From the label: indications

Colesevelam hydrochloride is a bile acid sequestrant indicated as an adjunct to diet and exercise to: reduce elevated low-density lipoprotein cholesterol (LDL-C) in adults with primary hyperlipidemia ( 1.1 ). reduce LDL-C levels in boys and postmenarchal girls, 10 to 17 years of age, with heterozygous familial hypercholesterolemia (HeFH), unable to reach LDL-C target levels despite an adequate trial of diet and lifestyle modification ( 1.1 ). improve glycemic control in adults with type 2 diabetes mellitus ( 1.2 ). […]

On the market

Earliest approval on file
May 26, 2000
Generic labelers
15 labelers
Pharmacy cost
$0.262 per tablet

Supply and safety

Shortage
No current entry
Recalls
1

Highlights of the cholestyramine record

Cholestyramine (Questran) · label of August 20, 2026

Used for

From the label: indications

Cholestyramine for oral suspension, USP powder is indicated as adjunctive therapy to diet for the reduction of elevated serum cholesterol in patients with primary hypercholesterolemia (elevated low-density lipoprotein [LDL] cholesterol) who do not respond adequately to diet. […]

On the market

Earliest approval on file
August 3, 1973
Generic labelers
15 labelers
Pharmacy cost
$0.834 per packet

Supply and safety

Shortage
No current entry
Recalls
0

Source: FDA drug labels via openFDA (Colesevelam label of December 28, 2023, Cholestyramine label of August 20, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do colesevelam and cholestyramine differ on the record?

How each works, in its label's words: Colesevelam, “Primary Hyperlipidemia: Colesevelam hydrochloride, the active pharmaceutical ingredient, is a non-absorbed, lipid-lowering polymer that binds bile acids in the intestine, impeding their reabsorption.”; Cholestyramine, “and an effect on serum lipids similar to that of cholestyramine for oral suspension) plus either nicotinic acid or lovastatin.”

Both are in FDA's class bile acid sequestrants.

Generics: colesevelam since 2018; cholestyramine since 1996 (Drugs@FDA).

ColesevelamCholestyramine
Labeled forHigh cholesterol, Type 2 diabetesHigh cholesterol
Pharmacologic classBile Acid SequestrantBile Acid Sequestrant
How it works (label)Primary Hyperlipidemia: Colesevelam hydrochloride, the active pharmaceutical ingredient, is a non-absorbed, lipid-lowering polymer that binds bile acids in the intestine, impeding their reabsorption.and an effect on serum lipids similar to that of cholestyramine for oral suspension) plus either nicotinic acid or lovastatin.
Half-life (label)n/an/a
Earliest approval on file (Drugs@FDA)May 26, 2000August 3, 1973
First generic approvedMay 16, 2018February 22, 1996
Generic labelers (NDC)15 labelers15 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$0.262 per tablet (Colesevelam 625 mg tablet)$0.834 per packet (Cholestyramine packet)
12-month price change-2%-5%
Boxed warningNoNo
Shortage nowNo current entryNo current entry
Recalls recorded10
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)2,01312,024
DEA schedulenonenone

Source: Drugs@FDA, FDA NDC Directory, CMS NADAC of October 7, 2026, FDA shortages and recalls, FAERS via openFDA (FDA files October 8, 2026)

What next?

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