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
72888-104_4b921bb1-ab2e-af6a-e063-6294a90a0694
Product NDC
72888-104
Form
SOLUTION
Composition / generic term
gabapentin
Labeler
Advagen Pharma Ltd
Marketing category
ANDA
Marketing start / end (source format)
20230118
Source listing expiry
20271231

Source-listed ingredients

  • GABAPENTIN — 250 mg/5mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 470 mL in 1 BOTTLE (72888-104-25) · 72888-104-25

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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