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
- 67877-222_f1432ab9-9c63-4880-8c9b-b851c16dc765
- Product NDC
- 67877-222
- Form
- CAPSULE
- Composition / generic term
- Gabapentin
- Labeler
- Ascend Laboratories, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110129
- Source listing expiry
- 20271231
Source-listed ingredients
- GABAPENTIN — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BOTTLE (67877-222-01) · 67877-222-01
- 500 CAPSULE in 1 BOTTLE (67877-222-05) · 67877-222-05
- 1000 CAPSULE in 1 BOTTLE (67877-222-10) · 67877-222-10
- 10 BLISTER PACK in 1 CARTON (67877-222-38) / 10 CAPSULE in 1 BLISTER PACK · 67877-222-38
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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