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
87441-036_54edde42-4bba-0668-e063-6294a90abd16
Product NDC
87441-036
Form
TABLET
Composition / generic term
Gabapentin
Labeler
Unit Dose Solutions, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20260623
Source listing expiry
20271231

Source-listed ingredients

  • GABAPENTIN — 600 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BLISTER PACK (87441-036-01) · 87441-036-01

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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