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Two medicines, side by side

Pregabalin vs clonazepam

Pregabalin and clonazepam are both labeled for seizures and epilepsy. Drugs@FDA records approvals of pregabalin since 2004 and of clonazepam since 1975. Pharmacies paid $0.0571 per pregabalin 100 mg capsule and $0.0244 per clonazepam 1 mg tablet (NADAC, October 7, 2026); the strengths differ, so the two prices are not like for like. Only the clonazepam label carries a boxed warning.

Check it at the source: the pregabalin FDA label on DailyMed (effective April 15, 2025); the clonazepam FDA label on DailyMed (effective December 1, 2025).

Highlights of the pregabalin record

Pregabalin (Lyrica) · label of April 15, 2025

Used for

From the label: indications

LYRICA is indicated for: • Management of neuropathic pain associated with diabetic peripheral neuropathy • Management of postherpetic neuralgia • Adjunctive therapy for the treatment of partial‑onset seizures in patients 1 month of age and older • Management of fibromyalgia • Management of neuropathic pain associated with spinal cord injury LYRICA is indicated for: • Neuropathic pain associated with diabetic […]

On the market

Earliest approval on file
December 30, 2004
Generic labelers
52 labelers
Pharmacy cost
$0.0571 per capsule

Supply and safety

Shortage
No current entry
Recalls
5

Highlights of the clonazepam record

Clonazepam (Klonopin) · label of December 1, 2025

Boxed warning

RISKS FROM CONCOMITANT USE WITH OPIOIDS; ABUSE, MISUSE, AND ADDICTION; and DEPENDENCE AND WITHDRAWAL REACTIONS Concomitant use of benzodiazepines and opioids may result in profound sedation, respiratory depression, coma, and death. Reserve concomitant prescribing of these drugs for patients for whom alternative treatment options are inadequate. Limit dosages and durations to the minimum required.

Used for

From the label: indications

Seizure Disorders Klonopin is useful alone or as an adjunct in the treatment of the Lennox-Gastaut syndrome (petit mal variant), akinetic, and myoclonic seizures. In patients with absence seizures (petit mal) who have failed to respond to succinimides, Klonopin may be useful. Some loss of effect may occur during the course of clonazepam treatment (see PRECAUTIONS: Loss of Effect ). […]

On the market

Earliest approval on file
June 4, 1975
Generic labelers
31 labelers
Pharmacy cost
$0.0244 per tablet

Supply and safety

Shortage
In shortage
Recalls
7

Source: FDA drug labels via openFDA (Pregabalin label of April 15, 2025, Clonazepam label of December 1, 2025); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do pregabalin and clonazepam differ on the record?

Only the clonazepam label carries a boxed warning.

Half-life, in each label's words: Pregabalin, “12.3 Pharmacokinetics Pregabalin is well absorbed after oral administration, is eliminated largely by renal excretion …”; Clonazepam, “The elimination half-life of clonazepam is typically 30 to 40 hours.”

Generics: pregabalin since 2019; clonazepam since 1996 (Drugs@FDA).

DEA schedule: pregabalin CV; clonazepam CIV.

PregabalinClonazepam
Labeled forNerve pain and fibromyalgia, Seizures and epilepsySeizures and epilepsy, Anxiety
Pharmacologic classn/aBenzodiazepine
How it works (label)LYRICA (pregabalin) binds with high affinity to the alpha 2 -delta site (an auxiliary subunit of voltage-gated calcium channels) in central nervous system tissues.n/a
Half-life (label)12.3 Pharmacokinetics Pregabalin is well absorbed after oral administration, is eliminated largely by renal excretion, and has an elimination half-life of about 6 hours.The elimination half-life of clonazepam is typically 30 to 40 hours.
Earliest approval on file (Drugs@FDA)December 30, 2004June 4, 1975
First generic approvedJuly 19, 2019September 10, 1996
Generic labelers (NDC)52 labelers31 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$0.0571 per capsule (Pregabalin 100 mg capsule)$0.0244 per tablet (Clonazepam 1 mg tablet)
12-month price change-15%-14%
Boxed warningNoYes
Shortage nowNo current entryIn shortage
Recalls recorded57
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)270,624159,283
DEA scheduleCVCIV

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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