United States · FDA National Drug Code directory

Gabapentin

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
86211-112_63a5fc6d-ca57-4726-b70d-805ac023d959
Product NDC
86211-112
Form
SOLUTION
Composition / generic term
Gabapentin
Labeler
JVET PHARMACEUTICALS LLC
Marketing category
ANDA
Marketing start / end (source format)
20251215
Source listing expiry
20261231

Source-listed ingredients

  • GABAPENTIN — 250 mg/5mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 473 mL in 1 BOTTLE (86211-112-01) · 86211-112-01

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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