United States · FDA National Drug Code directory

Neurontin

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
58151-284_2d43f32d-2d96-4011-84ac-507c3307dc27
Product NDC
58151-284
Form
TABLET, FILM COATED
Composition / generic term
gabapentin
Labeler
Viatris Specialty LLC
Marketing category
NDA
Marketing start / end (source format)
20251001
Source listing expiry
20271231

Source-listed ingredients

  • GABAPENTIN — 600 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET, FILM COATED in 1 BOTTLE (58151-284-01) · 58151-284-01

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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