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
76282-321_5e0a57d7-9068-43d3-be26-96f646720fde
Product NDC
76282-321
Form
CAPSULE
Composition / generic term
GABAPENTIN
Labeler
Exelan Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20100426
Source listing expiry
20261231

Source-listed ingredients

  • GABAPENTIN — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 CAPSULE in 1 BOTTLE (76282-321-01) · 76282-321-01
  • 500 CAPSULE in 1 BOTTLE (76282-321-05) · 76282-321-05
  • 180 CAPSULE in 1 BOTTLE (76282-321-18) · 76282-321-18
  • 270 CAPSULE in 1 BOTTLE (76282-321-27) · 76282-321-27
  • 90 CAPSULE in 1 BOTTLE (76282-321-90) · 76282-321-90

Source and coverage

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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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