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
- 62756-139_ca2658ac-c659-4217-8625-a1043d211cd5
- Product NDC
- 62756-139
- Form
- CAPSULE
- Composition / generic term
- gabapentin
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220201
- Source listing expiry
- 20271231
Source-listed ingredients
- GABAPENTIN — 400 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 50 CAPSULE in 1 BOX, UNIT-DOSE (62756-139-01) · 62756-139-01
- 100 CAPSULE in 1 BOTTLE (62756-139-03) · 62756-139-03
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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