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
- 16714-663_2f6c168b-aaf3-4a6a-b8a0-5be6b5f81d7e
- Product NDC
- 16714-663
- Form
- CAPSULE
- Composition / generic term
- Gabapentin
- Labeler
- NorthStar Rx LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20080131
- Source listing expiry
- 20261231
Source-listed ingredients
- GABAPENTIN — 400 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BOTTLE (16714-663-01) · 16714-663-01
- 500 CAPSULE in 1 BOTTLE (16714-663-02) · 16714-663-02
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →