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
- 71335-2719_e32af642-d4a8-4554-b512-75bdc8790ac8
- Product NDC
- 71335-2719
- Form
- TABLET, FILM COATED
- Composition / generic term
- Gabapentin
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20111006
- Source listing expiry
- 20261231
Source-listed ingredients
- GABAPENTIN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET, FILM COATED in 1 BOTTLE (71335-2719-1) · 71335-2719-1
- 58 TABLET, FILM COATED in 1 BOTTLE (71335-2719-2) · 71335-2719-2
- 100 TABLET, FILM COATED in 1 BOTTLE (71335-2719-3) · 71335-2719-3
- 120 TABLET, FILM COATED in 1 BOTTLE (71335-2719-4) · 71335-2719-4
- 60 TABLET, FILM COATED in 1 BOTTLE (71335-2719-5) · 71335-2719-5
- 30 TABLET, FILM COATED in 1 BOTTLE (71335-2719-6) · 71335-2719-6
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 →