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
- 42385-979_5fd82a02-46ac-4312-a008-fa17e5cd3ffd
- Product NDC
- 42385-979
- Form
- TABLET, FILM COATED
- Composition / generic term
- Gabapentin
- Labeler
- Laurus Labs Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240409
- Source listing expiry
- 20271231
Source-listed ingredients
- GABAPENTIN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (42385-979-01) · 42385-979-01
- 500 TABLET, FILM COATED in 1 BOTTLE (42385-979-05) · 42385-979-05
- 1000 TABLET, FILM COATED in 1 BOTTLE (42385-979-11) · 42385-979-11
- 30 TABLET, FILM COATED in 1 BOTTLE (42385-979-30) · 42385-979-30
- 10 BLISTER PACK in 1 CARTON (42385-979-72) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 42385-979-72
- 90 TABLET, FILM COATED in 1 BOTTLE (42385-979-90) · 42385-979-90
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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