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
- 68094-069_9c1384ca-7455-42ac-9f53-dddc6e995595
- Product NDC
- 68094-069
- Form
- TABLET, COATED
- Composition / generic term
- Gabapentin
- Labeler
- Precision Dose, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260105
- Source listing expiry
- 20271231
Source-listed ingredients
- GABAPENTIN — 600 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 BLISTER PACK in 1 CARTON (68094-069-61) / 10 TABLET, COATED in 1 BLISTER PACK (68094-069-59) · 68094-069-61
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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