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
- 71335-1200_4be0d60b-e4d2-484b-a870-6fdc3893f5f9
- Product NDC
- 71335-1200
- Form
- TABLET
- Composition / generic term
- Gabapentin
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20151101
- Source listing expiry
- 20261231
Source-listed ingredients
- GABAPENTIN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 28 TABLET in 1 BOTTLE (71335-1200-0) · 71335-1200-0
- 30 TABLET in 1 BOTTLE (71335-1200-1) · 71335-1200-1
- 60 TABLET in 1 BOTTLE (71335-1200-2) · 71335-1200-2
- 180 TABLET in 1 BOTTLE (71335-1200-3) · 71335-1200-3
- 90 TABLET in 1 BOTTLE (71335-1200-4) · 71335-1200-4
- 100 TABLET in 1 BOTTLE (71335-1200-5) · 71335-1200-5
- 120 TABLET in 1 BOTTLE (71335-1200-6) · 71335-1200-6
- 500 TABLET in 1 BOTTLE (71335-1200-7) · 71335-1200-7
- 84 TABLET in 1 BOTTLE (71335-1200-8) · 71335-1200-8
- 112 TABLET in 1 BOTTLE (71335-1200-9) · 71335-1200-9
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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