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
- 71205-932_26bd4975-008b-4029-b0da-3a75b0f7e0f4
- Product NDC
- 71205-932
- Form
- TABLET
- Composition / generic term
- Gabapentin
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160411
- Source listing expiry
- 20261231
Source-listed ingredients
- GABAPENTIN — 800 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (71205-932-00) · 71205-932-00
- 30 TABLET in 1 BOTTLE (71205-932-30) · 71205-932-30
- 500 TABLET in 1 BOTTLE (71205-932-55) · 71205-932-55
- 60 TABLET in 1 BOTTLE (71205-932-60) · 71205-932-60
- 240 TABLET in 1 BOTTLE (71205-932-64) · 71205-932-64
- 270 TABLET in 1 BOTTLE (71205-932-67) · 71205-932-67
- 120 TABLET in 1 BOTTLE (71205-932-72) · 71205-932-72
- 360 TABLET in 1 BOTTLE (71205-932-76) · 71205-932-76
- 180 TABLET in 1 BOTTLE (71205-932-78) · 71205-932-78
- 90 TABLET in 1 BOTTLE (71205-932-90) · 71205-932-90
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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