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
- 76282-405_20a38b18-352b-47a6-b640-091b42db10aa
- Product NDC
- 76282-405
- Form
- TABLET, FILM COATED
- Composition / generic term
- gabapentin
- Labeler
- Exelan Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20121102
- Source listing expiry
- 20261231
Source-listed ingredients
- GABAPENTIN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (76282-405-01) · 76282-405-01
- 500 TABLET, FILM COATED in 1 BOTTLE (76282-405-05) · 76282-405-05
- 30 TABLET, FILM COATED in 1 BOTTLE (76282-405-30) · 76282-405-30
- 90 TABLET, FILM COATED in 1 BOTTLE (76282-405-90) · 76282-405-90
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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