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
- 71335-1601_d10ce738-791e-49e4-833a-6714945746b5
- Product NDC
- 71335-1601
- Form
- TABLET, FILM COATED
- Composition / generic term
- GABAPENTIN
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140111
- Source listing expiry
- 20271231
Source-listed ingredients
- GABAPENTIN — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-1601-1) · 71335-1601-1
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-1601-2) · 71335-1601-2
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-1601-3) · 71335-1601-3
- 180 TABLET, FILM COATED in 1 BOTTLE (71335-1601-4) · 71335-1601-4
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-1601-5) · 71335-1601-5
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-1601-6) · 71335-1601-6
- 84 TABLET, FILM COATED in 1 BOTTLE (71335-1601-7) · 71335-1601-7
- 112 TABLET, FILM COATED in 1 BOTTLE (71335-1601-8) · 71335-1601-8
- 135 TABLET, FILM COATED in 1 BOTTLE (71335-1601-9) · 71335-1601-9
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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