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
- 71335-0351_165c2908-0442-46aa-82e6-4c4ad348a0d1
- Product NDC
- 71335-0351
- Form
- CAPSULE
- Composition / generic term
- Gabapentin
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140403
- Source listing expiry
- 20261231
Source-listed ingredients
- GABAPENTIN — 400 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 180 CAPSULE in 1 BOTTLE (71335-0351-0) · 71335-0351-0
- 20 CAPSULE in 1 BOTTLE (71335-0351-1) · 71335-0351-1
- 90 CAPSULE in 1 BOTTLE (71335-0351-2) · 71335-0351-2
- 60 CAPSULE in 1 BOTTLE (71335-0351-3) · 71335-0351-3
- 30 CAPSULE in 1 BOTTLE (71335-0351-4) · 71335-0351-4
- 120 CAPSULE in 1 BOTTLE (71335-0351-5) · 71335-0351-5
- 21 CAPSULE in 1 BOTTLE (71335-0351-6) · 71335-0351-6
- 84 CAPSULE in 1 BOTTLE (71335-0351-7) · 71335-0351-7
- 112 CAPSULE in 1 BOTTLE (71335-0351-8) · 71335-0351-8
- 28 CAPSULE in 1 BOTTLE (71335-0351-9) · 71335-0351-9
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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