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
71335-3140_b83b3496-b761-41ca-8a70-87642b9c9496
Product NDC
71335-3140
Form
CAPSULE
Composition / generic term
Gabapentin
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20160218
Source listing expiry
20271231

Source-listed ingredients

  • GABAPENTIN — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 CAPSULE in 1 BOTTLE (71335-3140-1) · 71335-3140-1
  • 28 CAPSULE in 1 BOTTLE (71335-3140-2) · 71335-3140-2
  • 30 CAPSULE in 1 BOTTLE (71335-3140-3) · 71335-3140-3
  • 60 CAPSULE in 1 BOTTLE (71335-3140-4) · 71335-3140-4
  • 120 CAPSULE in 1 BOTTLE (71335-3140-5) · 71335-3140-5
  • 84 CAPSULE in 1 BOTTLE (71335-3140-6) · 71335-3140-6

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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