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Two medicines, side by side

Primidone vs gabapentin

Primidone and gabapentin are both labeled for seizures and epilepsy. Drugs@FDA records approvals of primidone since 1954 and of gabapentin since 1993. Pharmacies paid $0.0914 per primidone 50 mg tablet and $0.0218 per gabapentin 100 mg capsule (NADAC, October 7, 2026); the strengths differ, so the two prices are not like for like. How each works, in its label's words: Primidone, “ACTIONS MYSOLINE raises electro- or chemoshock seizure thresholds or alters seizure patterns in experimental animals.”; Gabapentin, “The precise mechanisms by which gabapentin produces its analgesic and antiepileptic actions are unknown.”

Check it at the source: the primidone FDA label on DailyMed (effective September 10, 2026); the gabapentin FDA label on DailyMed (effective May 12, 2026).

Highlights of the primidone record

Primidone (Mysoline) · label of September 10, 2026

Used for

From the label: indications

MYSOLINE, used alone or concomitantly with other anticonvulsants, is indicated in the control of grand mal, psychomotor, and focal epileptic seizures. It may control grand mal seizures refractory to other anticonvulsant therapy.

On the market

Earliest approval on file
March 8, 1954
Generic labelers
21 labelers
Pharmacy cost
$0.0914 per tablet

Supply and safety

Shortage
No current entry
Recalls
6

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 (Primidone label of September 10, 2026, Gabapentin label of May 12, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do primidone and gabapentin differ on the record?

How each works, in its label's words: Primidone, “ACTIONS MYSOLINE raises electro- or chemoshock seizure thresholds or alters seizure patterns in experimental animals.”; Gabapentin, “The precise mechanisms by which gabapentin produces its analgesic and antiepileptic actions are unknown.”

Both are in FDA's class anti-epileptic agents.

Generics: primidone since 1978; gabapentin since 2003 (Drugs@FDA).

PrimidoneGabapentin
Labeled forSeizures and epilepsyNerve pain and fibromyalgia, Seizures and epilepsy
Pharmacologic classAnti-epileptic AgentAnti-epileptic Agent
How it works (label)ACTIONS MYSOLINE raises electro- or chemoshock seizure thresholds or alters seizure patterns in experimental animals. The mechanism(s) of primidone’s antiepileptic action is not known.The precise mechanisms by which gabapentin produces its analgesic and antiepileptic actions are unknown.
Half-life (label)n/aGabapentin elimination half-life is 5 to 7 hours and is unaltered by dose or following multiple dosing.
Earliest approval on file (Drugs@FDA)March 8, 1954December 30, 1993
First generic approvedDecember 1, 1978September 12, 2003
Generic labelers (NDC)21 labelers85 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$0.0914 per tablet (Primidone 50 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 recorded622
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)10,126362,654
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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