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Two medicines, side by side

Carisoprodol vs tizanidine

Carisoprodol and tizanidine are both labeled for muscle spasms and spasticity. Drugs@FDA records approvals of carisoprodol since 1959 and of tizanidine since 1996. Pharmacies paid $0.0706 per carisoprodol 350 mg tablet and $0.0331 per tizanidine HCl 4 mg tablet (NADAC, October 7, 2026); the strengths differ, so the two prices are not like for like. In FDA's classes, carisoprodol is a muscle relaxant and tizanidine a central alpha-2 adrenergic agonist.

Check it at the source: the carisoprodol FDA label on DailyMed (effective July 15, 2025); the tizanidine FDA label on DailyMed (effective January 2, 2026).

Highlights of the carisoprodol record

Carisoprodol (Soma) · label of July 15, 2025

Used for

From the label: indications

Carisoprodol tablets are indicated for the relief of discomfort associated with acute, painful musculoskeletal conditions in adults. […]

On the market

Earliest approval on file
April 9, 1959
Generic labelers
24 labelers
Pharmacy cost
$0.0706 per tablet

Supply and safety

Shortage
No current entry
Recalls
5

Highlights of the tizanidine record

Tizanidine (Zanaflex) · label of January 2, 2026

Used for

From the label: indications

Zanaflex is indicated for the treatment of spasticity in adults. Zanaflex is a central alpha-2-adrenergic agonist indicated for the treatment of spasticity.

On the market

Earliest approval on file
November 27, 1996
Generic labelers
49 labelers
Pharmacy cost
$0.0331 per tablet

Supply and safety

Shortage
No current entry
Recalls
9

Source: FDA drug labels via openFDA (Carisoprodol label of July 15, 2025, Tizanidine label of January 2, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do carisoprodol and tizanidine differ on the record?

In FDA's classes, carisoprodol is a muscle relaxant and tizanidine a central alpha-2 adrenergic agonist.

How each works, in its label's words: Carisoprodol, “The mechanism of action of carisoprodol in relieving discomfort associated with acute painful musculoskeletal conditions has not been clearly identified.”; Tizanidine, “Tizanidine is a central alpha-2-adrenergic receptor agonist and presumably reduces spasticity by increasing presynaptic inhibition of motor neurons.”

Half-life, in each label's words: Carisoprodol, “Excretion Carisoprodol is eliminated by both renal and non-renal routes with a terminal elimination half-life of …”; Tizanidine, “Elimination Metabolism Tizanidine has a half-life of approximately 2.5 hours (CV=33%).”

Generics: carisoprodol since 1979; tizanidine since 2002 (Drugs@FDA).

DEA schedule: carisoprodol CIV; tizanidine none.

CarisoprodolTizanidine
Labeled forMuscle spasms and spasticityMuscle spasms and spasticity
Pharmacologic classMuscle RelaxantCentral alpha-2 Adrenergic Agonist
How it works (label)The mechanism of action of carisoprodol in relieving discomfort associated with acute painful musculoskeletal conditions has not been clearly identified.Tizanidine is a central alpha-2-adrenergic receptor agonist and presumably reduces spasticity by increasing presynaptic inhibition of motor neurons. The effects of tizanidine are greatest on polysynaptic pathways.
Half-life (label)Excretion Carisoprodol is eliminated by both renal and non-renal routes with a terminal elimination half-life of approximately 2 hours.Elimination Metabolism Tizanidine has a half-life of approximately 2.5 hours (CV=33%).
Earliest approval on file (Drugs@FDA)April 9, 1959November 27, 1996
First generic approvedJune 12, 1979June 27, 2002
Generic labelers (NDC)24 labelers49 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$0.0706 per tablet (Carisoprodol 350 mg tablet)$0.0331 per tablet (Tizanidine HCl 4 mg tablet)
12-month price change+3%-12%
Boxed warningNoNo
Shortage nowNo current entryNo current entry
Recalls recorded59
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)18,96441,179
DEA scheduleCIVnone

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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