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
- 71335-1199_5cfa0741-44a1-4c57-b7a8-677fe37a8d09
- Product NDC
- 71335-1199
- Form
- CAPSULE
- Composition / generic term
- Gabapentin
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110129
- Source listing expiry
- 20271231
Source-listed ingredients
- GABAPENTIN — 400 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 180 CAPSULE in 1 BOTTLE (71335-1199-0) · 71335-1199-0
- 20 CAPSULE in 1 BOTTLE (71335-1199-1) · 71335-1199-1
- 90 CAPSULE in 1 BOTTLE (71335-1199-2) · 71335-1199-2
- 60 CAPSULE in 1 BOTTLE (71335-1199-3) · 71335-1199-3
- 30 CAPSULE in 1 BOTTLE (71335-1199-4) · 71335-1199-4
- 120 CAPSULE in 1 BOTTLE (71335-1199-5) · 71335-1199-5
- 21 CAPSULE in 1 BOTTLE (71335-1199-6) · 71335-1199-6
- 84 CAPSULE in 1 BOTTLE (71335-1199-7) · 71335-1199-7
- 112 CAPSULE in 1 BOTTLE (71335-1199-8) · 71335-1199-8
- 28 CAPSULE in 1 BOTTLE (71335-1199-9) · 71335-1199-9
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →