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
65862-198_7a45ad84-02a4-442d-8401-1a1495d084fa
Product NDC
65862-198
Form
CAPSULE
Composition / generic term
Gabapentin
Labeler
Aurobindo Pharma Limited
Marketing category
ANDA
Marketing start / end (source format)
20080131
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 (65862-198-01) · 65862-198-01
  • 500 CAPSULE in 1 BOTTLE (65862-198-05) · 65862-198-05
  • 10 BLISTER PACK in 1 CARTON (65862-198-10) / 10 CAPSULE in 1 BLISTER PACK · 65862-198-10
  • 180 CAPSULE in 1 BOTTLE (65862-198-18) · 65862-198-18
  • 270 CAPSULE in 1 BOTTLE (65862-198-27) · 65862-198-27
  • 90 CAPSULE in 1 BOTTLE (65862-198-90) · 65862-198-90
  • 1000 CAPSULE in 1 BOTTLE (65862-198-99) · 65862-198-99

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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