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
- 71610-044_a695e055-6531-4b51-969f-62165d703511
- Product NDC
- 71610-044
- Form
- TABLET, FILM COATED
- Composition / generic term
- GABAPENTIN
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140111
- Source listing expiry
- 20261231
Source-listed ingredients
- GABAPENTIN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (71610-044-30) · 71610-044-30
- 45 TABLET, FILM COATED in 1 BOTTLE (71610-044-45) · 71610-044-45
- 60 TABLET, FILM COATED in 1 BOTTLE (71610-044-53) · 71610-044-53
- 90 TABLET, FILM COATED in 1 BOTTLE (71610-044-60) · 71610-044-60
- 120 TABLET, FILM COATED in 1 BOTTLE (71610-044-70) · 71610-044-70
- 135 TABLET, FILM COATED in 1 BOTTLE (71610-044-73) · 71610-044-73
- 180 TABLET, FILM COATED in 1 BOTTLE (71610-044-80) · 71610-044-80
- 270 TABLET, FILM COATED in 1 BOTTLE (71610-044-92) · 71610-044-92
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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