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
- 68788-7774_9a21dd1d-c795-4e56-b930-55dbb9254b71
- Product NDC
- 68788-7774
- Form
- TABLET
- Composition / generic term
- Gabapentin
- Labeler
- Preferred Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200824
- 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 (68788-7774-1) · 68788-7774-1
- 30 TABLET in 1 BOTTLE (68788-7774-3) · 68788-7774-3
- 60 TABLET in 1 BOTTLE (68788-7774-6) · 68788-7774-6
- 120 TABLET in 1 BOTTLE (68788-7774-8) · 68788-7774-8
- 90 TABLET in 1 BOTTLE (68788-7774-9) · 68788-7774-9
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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