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
- 68071-2600_5a9ab462-65d1-0636-e063-6394a90ad173
- Product NDC
- 68071-2600
- Form
- CAPSULE
- Composition / generic term
- Gabapentin
- Labeler
- NuCare Pharmaceuticals,Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160218
- Source listing expiry
- 20271231
Source-listed ingredients
- GABAPENTIN — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE in 1 BOTTLE, PLASTIC (68071-2600-3) · 68071-2600-3
- 40 CAPSULE in 1 BOTTLE, PLASTIC (68071-2600-4) · 68071-2600-4
- 60 CAPSULE in 1 BOTTLE, PLASTIC (68071-2600-6) · 68071-2600-6
- 90 CAPSULE in 1 BOTTLE, PLASTIC (68071-2600-9) · 68071-2600-9
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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