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
- 71335-1287_1d171bd2-0093-4327-9111-e883bd241e8c
- Product NDC
- 71335-1287
- Form
- TABLET, COATED
- Composition / generic term
- Gabapentin
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190501
- Source listing expiry
- 20271231
Source-listed ingredients
- GABAPENTIN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 28 TABLET, COATED in 1 BOTTLE (71335-1287-0) · 71335-1287-0
- 30 TABLET, COATED in 1 BOTTLE (71335-1287-1) · 71335-1287-1
- 60 TABLET, COATED in 1 BOTTLE (71335-1287-2) · 71335-1287-2
- 180 TABLET, COATED in 1 BOTTLE (71335-1287-3) · 71335-1287-3
- 90 TABLET, COATED in 1 BOTTLE (71335-1287-4) · 71335-1287-4
- 100 TABLET, COATED in 1 BOTTLE (71335-1287-5) · 71335-1287-5
- 120 TABLET, COATED in 1 BOTTLE (71335-1287-6) · 71335-1287-6
- 500 TABLET, COATED in 1 BOTTLE (71335-1287-7) · 71335-1287-7
- 84 TABLET, COATED in 1 BOTTLE (71335-1287-8) · 71335-1287-8
- 112 TABLET, COATED in 1 BOTTLE (71335-1287-9) · 71335-1287-9
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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