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Two medicines, side by side

Lacosamide vs gabapentin

Lacosamide and gabapentin are both labeled for seizures and epilepsy. Drugs@FDA records approvals of lacosamide since 2008 and of gabapentin since 1993. Pharmacies paid $0.174 per lacosamide 100 mg tablet and $0.0218 per gabapentin 100 mg capsule (NADAC, October 7, 2026).

Check it at the source: the lacosamide FDA label on DailyMed (effective May 12, 2026); the gabapentin FDA label on DailyMed (effective May 12, 2026).

Highlights of the lacosamide record

Lacosamide (Vimpat) · label of May 12, 2026

Used for

From the label: indications

VIMPAT is indicated for: Treatment of partial-onset seizures in patients 1 month of age and older ( 1.1 ) Adjunctive therapy in the treatment of primary generalized tonic-clonic seizures in patients 4 years of age and older ( 1.2 ) 1.1 Partial-Onset Seizures VIMPAT is indicated for the treatment of partial-onset seizures in patients 1 month of age and older. 1.2 Primary Generalized Tonic-Clonic Seizures VIMPAT is indicated as adjunctive therapy in the treatment of primary generalized tonic-clonic seizures in patients 4 years of age and older. […]

On the market

Earliest approval on file
October 28, 2008
Generic labelers
57 labelers
Pharmacy cost
$0.174 per tablet

Supply and safety

Shortage
No current entry
Recalls
8

Highlights of the gabapentin record

Gabapentin (Neurontin) · label of May 12, 2026

Used for

From the label: indications

NEURONTIN ® is indicated for: • Management of postherpetic neuralgia in adults • Adjunctive therapy in the treatment of partial onset seizures, with and without secondary generalization, in adults and pediatric patients 3 years and older with epilepsy NEURONTIN is indicated for: • Postherpetic neuralgia in adults ( 1 ) • Adjunctive therapy in the treatment of partial onset seizures, with and without secondary generalization, in adults and pediatric patients 3 years and older with epilepsy […]

On the market

Earliest approval on file
December 30, 1993
Generic labelers
85 labelers
Pharmacy cost
$0.0218 per capsule

Supply and safety

Shortage
No current entry
Recalls
22

Source: FDA drug labels via openFDA (Lacosamide label of May 12, 2026, Gabapentin label of May 12, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do lacosamide and gabapentin differ on the record?

How each works, in its label's words: Lacosamide, “The precise mechanism by which VIMPAT exerts its antiepileptic effects in humans remains to be fully elucidated.”; Gabapentin, “The precise mechanisms by which gabapentin produces its analgesic and antiepileptic actions are unknown.”

Half-life, in each label's words: Lacosamide, “The maximum lacosamide plasma concentrations occur approximately 1-to-4-hour post-dose after oral dosing, and …”; Gabapentin, “Gabapentin elimination half-life is 5 to 7 hours and is unaltered by dose or following multiple dosing.”

Generics: lacosamide since 2022; gabapentin since 2003 (Drugs@FDA).

DEA schedule: lacosamide CV; gabapentin none.

LacosamideGabapentin
Labeled forSeizures and epilepsyNerve pain and fibromyalgia, Seizures and epilepsy
Pharmacologic classn/aAnti-epileptic Agent
How it works (label)The precise mechanism by which VIMPAT exerts its antiepileptic effects in humans remains to be fully elucidated.The precise mechanisms by which gabapentin produces its analgesic and antiepileptic actions are unknown.
Half-life (label)The maximum lacosamide plasma concentrations occur approximately 1-to-4-hour post-dose after oral dosing, and elimination half-life is approximately 13 hours.Gabapentin elimination half-life is 5 to 7 hours and is unaltered by dose or following multiple dosing.
Earliest approval on file (Drugs@FDA)October 28, 2008December 30, 1993
First generic approvedMarch 17, 2022September 12, 2003
Generic labelers (NDC)57 labelers85 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$0.174 per tablet (Lacosamide 100 mg tablet)$0.0218 per capsule (Gabapentin 100 mg capsule)
12-month price change-15%+0.9%
Boxed warningNoNo
Shortage nowNo current entryNo current entry
Recalls recorded822
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)36,995362,654
DEA scheduleCVnone

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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