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
- 63739-902_159496fe-700e-4c94-a766-7809a7ce1839
- Product NDC
- 63739-902
- Form
- CAPSULE
- Composition / generic term
- Gabapentin
- Labeler
- McKesson Corporation dba Sky Packaging
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210715
- Source listing expiry
- 20261231
Source-listed ingredients
- GABAPENTIN — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 BLISTER PACK in 1 CARTON (63739-902-10) / 10 CAPSULE in 1 BLISTER PACK · 63739-902-10
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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