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
- 71335-3057_6af55316-950c-402a-b479-4fdf6bc662cd
- Product NDC
- 71335-3057
- Form
- TABLET
- Composition / generic term
- Gabapentin
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20211001
- Source listing expiry
- 20271231
Source-listed ingredients
- GABAPENTIN — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71335-3057-1) · 71335-3057-1
- 60 TABLET in 1 BOTTLE (71335-3057-2) · 71335-3057-2
- 90 TABLET in 1 BOTTLE (71335-3057-3) · 71335-3057-3
- 180 TABLET in 1 BOTTLE (71335-3057-4) · 71335-3057-4
- 120 TABLET in 1 BOTTLE (71335-3057-5) · 71335-3057-5
- 100 TABLET in 1 BOTTLE (71335-3057-6) · 71335-3057-6
- 84 TABLET in 1 BOTTLE (71335-3057-7) · 71335-3057-7
- 112 TABLET in 1 BOTTLE (71335-3057-8) · 71335-3057-8
- 135 TABLET in 1 BOTTLE (71335-3057-9) · 71335-3057-9
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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